(Q37675919)

21 August 2017

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title

Molecular basis of hereditary cardiomyopathy: abnormalities in calcium sensitivity, stretch response, stress response and beyond (English)

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21 August 2017

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Akinori Kimura

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21 August 2017

language of work or name

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15 January 2010

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Journal of Human Genetics

21 August 2017

published in

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21 August 2017

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21 August 2017

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21 August 2017

page(s)

81-90

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https://api.crossref.org/works/10.1038%2FJHG.2009.138

21 August 2017

1 reference

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

The genetic basis for cardiac remodeling

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Restrictive Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

The Genetic Basis for Cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Frequency of familial dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Phenotypic diversity in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Molecular etiology and pathogenesis of hereditary cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

A missense mutation of cardiac beta-myosin heavy chain gene linked to familial hypertrophic cardiomyopathy in affected Japanese families

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Clinical manifestations of hypertrophic cardiomyopathy with mutations in the cardiac beta-myosin heavy chain gene or cardiac troponin T gene

21 January 2018

2 references

https://api.crossref.org/works/10.1038%2FJHG.2009.138

21 January 2018

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

Structural interpretation of the mutations in the beta-cardiac myosin that have been implicated in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mutations in the genes for cardiac troponin T and alpha-tropomyosin in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Lifelong left ventricular remodeling of hypertrophic cardiomyopathy caused by a founder frameshift deletion mutation in the cardiac Myosin-binding protein C gene among Japanese

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

A Mutant Tropomyosin That Causes Hypertrophic Cardiomyopathy Is Expressed In Vivo and Associated With an Increased Calcium Sensitivity

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Altered regulatory properties of human cardiac troponin I mutants that cause hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Hypercontractile properties of cardiac muscle fibers in a knock-in mouse model of cardiac myosin-binding protein-C

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mechanical defects of muscle fibers with myosin light chain mutants that cause cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

A functional and structural study of troponin C mutations related to hypertrophic cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Single-molecule mechanics of R403Q cardiac myosin isolated from the mouse model of familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Structural analysis of the titin gene in hypertrophic cardiomyopathy: identification of a novel disease gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Tcap gene mutations in hypertrophic cardiomyopathy and dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Titin isoform-dependent effect of calcium on passive myocardial tension

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Length-dependent Ca(2+) activation in cardiac muscle: some remaining questions

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mutations in the human muscle LIM protein gene in families with hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Decreased interactions of mutant muscle LIM protein (MLP) with N-RAP and alpha-actinin and their implication for hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mutations in the muscle LIM protein and α-actinin-2 genes in dilated cardiomyopathy and endocardial fibroelastosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Identification and functional analysis of a caveolin-3 mutation associated with familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mutations in JPH2-encoded junctophilin-2 associated with hypertrophic cardiomyopathy in humans

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Structural analysis of obscurin gene in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Cardiac ankyrin repeat protein gene (ANKRD1) mutations in hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Human alpha B-crystallin mutation causes oxido-reductive stress and protein aggregation cardiomyopathy in mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Alpha B-crystallin mutation in dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Behavior of caveolae and caveolin-3 during the development of myocyte hypertrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Adenovirus-mediated overexpression of caveolin-3 inhibits rat cardiomyocyte hypertrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Obscurin, a giant sarcomeric Rho guanine nucleotide exchange factor protein involved in sarcomere assembly

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Cardiac ankyrin repeat protein is a novel marker of cardiac hypertrophy: role of M-CAT element within the promoter

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Multiple pathogenetic mechanisms in X linked dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Dystrophin and mutations: one gene, several proteins, multiple phenotypes

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

The heart in human dystrophinopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

The dystrophin glycoprotein complex: signaling strength and integrity for the sarcolemma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mutations in the human delta-sarcoglycan gene in familial and sporadic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Laminin-alpha4 and integrin-linked kinase mutations cause human cardiomyopathy via simultaneous defects in cardiomyocytes and endothelial cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Genetic abnormalities responsible for dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Actin mutations in dilated cardiomyopathy, a heritable form of heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Alpha-cardiac actin is a novel disease gene in familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Actin mutations in hypertrophic and dilated cardiomyopathy cause inefficient protein folding and perturbed filament formation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Ca(2+)-desensitizing effect of a deletion mutation Delta K210 in cardiac troponin T that causes familial dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Sarcomeric protein mutations in dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Titin mutations as the molecular basis for dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

The cardiac mechanical stretch sensor machinery involves a Z disc complex that is defective in a subset of human dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Cypher, a striated muscle-restricted PDZ and LIM domain-containing protein, binds to alpha-actinin-2 and protein kinase C

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Calsarcins, a novel family of sarcomeric calcineurin-binding proteins

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Calcium-calcineurin signaling in the regulation of cardiac hypertrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Regulation of cardiac hypertrophy by intracellular signalling pathways

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Attenuation of cardiac remodeling after myocardial infarction by muscle LIM protein-calcineurin signaling at the sarcomeric Z-disc

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

A Cypher/ZASP mutation associated with dilated cardiomyopathy alters the binding affinity to protein kinase C.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mutations in Cypher/ZASP in patients with dilated cardiomyopathy and left ventricular non-compaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Impaired binding of ZASP/Cypher with phosphoglucomutase 1 is associated with dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Desmin mutation responsible for idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Metavinculin mutations alter actin interaction in dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Early and sustained benefit on event-free survival and heart failure hospitalization from fixed-dose combination of isosorbide dinitrate/hydralazine: consistency across subgroups in the African-American Heart Failure Trial

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mutations in the Z-band protein myopalladin gene and idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Identification of new mutations in the Emery-Dreifuss muscular dystrophy gene and evidence for genetic heterogeneity of the disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Heart to heart: from nuclear proteins to Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Lamin A/C and cardiac diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Activation of MAPK pathways links LMNA mutations to cardiomyopathy in Emery-Dreifuss muscular dystrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

ABCC9 mutations identified in human dilated cardiomyopathy disrupt catalytic KATP channel gating

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

SCN5A mutation associated with dilated cardiomyopathy, conduction disorder, and arrhythmia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Inherited arrhythmias: a National Heart, Lung, and Blood Institute and Office of Rare Diseases workshop consensus report about the diagnosis, phenotyping, molecular mechanisms, and therapeutic approaches for primary cardiomyopathies of gene mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Structural analysis of four and half LIM protein-2 in dilated cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

The multifunctional roles of the four-and-a-half-LIM only protein FHL2.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

ANKRD1, the gene encoding cardiac ankyrin repeat protein, is a novel dilated cardiomyopathy gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Reversal of calcium cycling defects in advanced heart failure toward molecular therapy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Dilated cardiomyopathy and heart failure caused by a mutation in phospholamban

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

A mutation in the human phospholamban gene, deleting arginine 14, results in lethal, hereditary cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Genetic screening of calcium regulation genes in familial hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Chronic phospholamban-sarcoplasmic reticulum calcium ATPase interaction is the critical calcium cycling defect in dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Chronic suppression of heart-failure progression by a pseudophosphorylated mutant of phospholamban via in vivo cardiac rAAV gene delivery

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Identification of the Syrian hamster cardiomyopathy gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mutational screening of phospholamban gene in hypertrophic and idiopathic dilated cardiomyopathy and functional study of the PLN -42 C>G mutation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Cardiac-specific overexpression of phospholamban alters calcium kinetics and resultant cardiomyocyte mechanics in transgenic mice

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

X-linked cardioskeletal myopathy and neutropenia (Barth syndrome): an update

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Fukutin gene mutations cause dilated cardiomyopathy with minimal muscle weakness

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Loss of desmoplakin isoform I causes early onset cardiomyopathy and heart failure in a Naxos-like syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mutational analysis of fukutin gene in dilated cardiomyopathy and hypertrophic cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

A troponin T mutation that causes infantile restrictive cardiomyopathy increases Ca2+ sensitivity of force development and impairs the inhibitory properties of troponin

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Drastic Ca2+ sensitization of myofilament associated with a small structural change in troponin I in inherited restrictive cardiomyopathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Idiopathic restrictive cardiomyopathy is part of the clinical expression of cardiac troponin I mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Noncompaction of the ventricular myocardium is associated with a de novo mutation in the beta-myosin heavy chain gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mutation in the alpha-cardiac actin gene associated with apical hypertrophic cardiomyopathy, left ventricular non-compaction, and septal defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Familial dilated cardiomyopathy and isolated left ventricular noncompaction associated with lamin A/C gene mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Neonatal, lethal noncompaction of the left ventricular myocardium is allelic with Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Novel gene mutations in patients with left ventricular noncompaction or Barth syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

BMP10 is essential for maintaining cardiac growth during murine cardiogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Heart specific expression of mouse BMP-10 a novel member of the TGF-beta superfamily

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Interaction of BMP10 with Tcap may modulate the course of hypertensive cardiac hypertrophy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Molecular genetics of arrhythmogenic right ventricular cardiomyopathy: emerging horizon?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Identification of a deletion in plakoglobin in arrhythmogenic right ventricular cardiomyopathy with palmoplantar keratoderma and woolly hair (Naxos disease).

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

A recessive mutation in desmoplakin causes arrhythmogenic right ventricular dysplasia, skin disorder, and woolly hair

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Mutations in desmoglein-2 gene are associated with arrhythmogenic right ventricular cardiomyopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Identification of mutations in the cardiac ryanodine receptor gene in families affected with arrhythmogenic right ventricular cardiomyopathy type 2 (ARVD2)

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Regulatory mutations in transforming growth factor-beta3 gene cause arrhythmogenic right ventricular cardiomyopathy type 1

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

SCH00013, a novel Ca(2+) sensitizer with positive inotropic and no chronotropic action in heart failure

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

Prevalence, Clinical Significance, and Genetic Basis of Hypertrophic Cardiomyopathy With Restrictive Phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

The genetic basis for cardiomyopathy: from mutation identification to mechanistic paradigms

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

Familial dilated cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

Possible gene dose effect of a mutant cardiac beta-myosin heavy chain gene on the clinical expression of familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

Characteristics and prognostic implications of myosin missense mutations in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

Early expression of a malignant phenotype of familial hypertrophic cardiomyopathy associated with a Gly716Arg myosin heavy chain mutation in a Korean family

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

A myosin missense mutation, not a null allele, causes familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

Hypertrophic cardiomyopathy: histopathological features of sudden death in cardiac troponin T disease

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

Ca2+ sensitization and potentiation of the maximum level of myofibrillar ATPase activity caused by mutations of troponin T found in familial hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

Titin-based modulation of calcium sensitivity of active tension in mouse skinned cardiac myocytes

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

A missense mutation in a ubiquitously expressed protein, vinculin, confers susceptibility to hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

Expression of R120G-alphaB-crystallin causes aberrant desmin and alphaB-crystallin aggregation and cardiomyopathy in mice

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

Functional analysis of titin/connectin N2-B mutations found in cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

X-linked dilated cardiomyopathy. Molecular genetic evidence of linkage to the Duchenne muscular dystrophy (dystrophin) gene at the Xp21 locus

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

Prevalence of Desmin Mutations in Dilated Cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

Mouse model carrying H222P- Lmna mutation develops muscular dystrophy and dilated cardiomyopathy similar to human striated muscle laminopathies

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

The relative phospholamban and SERCA2 ratio: a critical determinant of myocardial contractility

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

Mutation of the phospholamban promoter associated with hypertrophic cardiomyopathy

1 reference

https://api.crossref.org/works/10.1038%2FJHG.2009.138

7 January 2021

Identifiers

DOI

10.1038/JHG.2009.138

1 reference

21 August 2017

1 reference