A gene locus for progressive familial heart block type II (PFHBII) maps to chromosome 1q32.2-q32.3. (Q39002730)

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scientific article published on 28 October 2005

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English	A gene locus for progressive familial heart block type II (PFHBII) maps to chromosome 1q32.2-q32.3.	scientific article published on 28 October 2005

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Europe PubMed Central

PubMed publication ID

16086176

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8 September 2017

title

A gene locus for progressive familial heart block type II (PFHBII) maps to chromosome 1q32.2-q32.3. (English)

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Europe PubMed Central

PubMed publication ID

16086176

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8 September 2017

main subject

progressive familial heart block type II

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author name string

Pedro Fernandez

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1

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Europe PubMed Central

PubMed publication ID

16086176

retrieved

8 September 2017

Johanna Moolman-Smook

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2

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Europe PubMed Central

PubMed publication ID

16086176

retrieved

8 September 2017

Paul Brink

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3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16086176

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8 September 2017

Valerie Corfield

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4

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Europe PubMed Central

PubMed publication ID

16086176

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8 September 2017

publication date

28 October 2005

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Europe PubMed Central

PubMed publication ID

16086176

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8 September 2017

published in

Human Genetics

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Europe PubMed Central

PubMed publication ID

16086176

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8 September 2017

volume

118

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Europe PubMed Central

PubMed publication ID

16086176

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8 September 2017

issue

1

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Europe PubMed Central

PubMed publication ID

16086176

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8 September 2017

page(s)

133-137

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Europe PubMed Central

PubMed publication ID

16086176

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8 September 2017

cites work

Genotype, phenotype: upstairs, downstairs in the family of cardiomyopathies

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Crossref

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https://api.crossref.org/works/10.1007%2FS00439-005-0029-5

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21 January 2018

Clinical and pathologic study of familial dilated cardiomyopathy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Severe disease expression of cardiac troponin C and T mutations in patients with idiopathic dilated cardiomyopathy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

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inferred from PubMed ID database lookup

Progressive familial heart block type II (PFHBII): a clinical profile from 1977 to 2003

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

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inferred from PubMed ID database lookup

Prediction of the coding sequences of unidentified human genes. VI. The coding sequences of 80 new genes (KIAA0201-KIAA0280) deduced by analysis of cDNA clones from cell line KG-1 and brain

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

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inferred from PubMed ID database lookup

The failing heart

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

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The complete primary structure for a novel laminin chain, the laminin B1k chain

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

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inferred from PubMed ID database lookup

Genomic rearrangements of EYA1 account for a large fraction of families with BOR syndrome

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

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inferred from PubMed ID database lookup

Genetics of atrioventricular conduction disease in humans

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

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inferred from PubMed ID database lookup

Sensitivity of lod scores to changes in diagnostic status

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

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inferred from PubMed ID database lookup

Mutations in the gamma(2) subunit of AMP-activated protein kinase cause familial hypertrophic cardiomyopathy: evidence for the central role of energy compromise in disease pathogenesis

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel mutations in sarcomeric protein genes in dilated cardiomyopathy.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

New phenotype of familial dilated cardiomyopathy and conduction disorders

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evidence-based diagnosis of familial non-X-linked dilated cardiomyopathy. Prevalence, inheritance and characteristics

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

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inferred from PubMed ID database lookup

Progressive familial heart block--two types

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cloning of a human ether-a-go-go potassium channel expressed in myoblasts at the onset of fusion

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

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inferred from PubMed ID database lookup

Easy calculations of lod scores and genetic risks on small computers

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Evolution of a hereditary cardiac conduction and muscle disorder: a study involving a family with six generations affected

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a new family of protein phosphatase 2A regulatory subunits

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymerase chain reaction-based detection of MN blood group-specific sequences in the human genome

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

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Molecular Genetics of Arrhythmias and Cardiovascular Conditions Associated with Arrhythmias

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16086176

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16086176

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel cardiac troponin T mutation as a cause of familial dilated cardiomyopathy

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/16086176

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/S00439-005-0029-5

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16086176

retrieved

8 September 2017

PubMed publication ID

16086176

1 reference

stated in

Europe PubMed Central

PubMed publication ID

16086176

retrieved

8 September 2017

 

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