High prevalence of Arginine to Glutamine substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians (Q34372769)

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English	High prevalence of Arginine to Glutamine substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians	scientific article

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22876777

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title

High prevalence of Arginine to Glutamine substitution at 98, 141 and 162 positions in Troponin I (TNNI3) associated with hypertrophic cardiomyopathy among Indians (English)

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22876777

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1 August 2017

main subject

hypertrophic cardiomyopathy

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author

Kumarasamy Thangaraj

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6

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22876777

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1 August 2017

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Deepa Selvi Rani

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1

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22876777

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1 August 2017

Pratibha Nallari

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2

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22876777

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1 August 2017

Singh Priyamvada

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3

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22876777

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1 August 2017

Calambur Narasimhan

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4

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22876777

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1 August 2017

Lalji Singh

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5

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22876777

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1 August 2017

publication date

10 August 2012

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22876777

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1 August 2017

published in

BMC Medical Genetics

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22876777

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1 August 2017

volume

13

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22876777

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1 August 2017

page(s)

69

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22876777

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1 August 2017

cites work

Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy

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A common MYBPC3 (cardiac myosin binding protein C) variant associated with cardiomyopathies in South Asia

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6 July 2018

MYBPC3 gene variations in hypertrophic cardiomyopathy patients in India

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6 July 2018

A second generation human haplotype map of over 3.1 million SNPs

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6 July 2018

Frequency and clinical expression of cardiac troponin I mutations in 748 consecutive families with hypertrophic cardiomyopathy.

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The relationship between synonymous codon usage and protein structure in Escherichia coli and Homo sapiens.

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Expression patterns and gene distribution in the human genome

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Hypertrophic cardiomyopathy: a systematic review

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Sarcomere protein gene mutations in hypertrophic cardiomyopathy of the elderly

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6 July 2018

Mutations in the cardiac troponin I gene associated with hypertrophic cardiomyopathy

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6 July 2018

Isolation and characterization of the human cardiac troponin I gene (TNNI3)

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Codon catalog usage and the genome hypothesis

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RNA splice junctions of different classes of eukaryotes: sequence statistics and functional implications in gene expression

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Splice junctions, branch point sites, and exons: sequence statistics, identification, and applications to genome project

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6 July 2018

Novel mutation in cardiac troponin I in recessive idiopathic dilated cardiomyopathy

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https://api.crossref.org/works/10.1186%2F1471-2350-13-69

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21 January 2018

Prevalence and spectrum of thin filament mutations in an outpatient referral population with hypertrophic cardiomyopathy

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21 January 2018

CAG repeat variation in the mtDNA polymerase γ is not associated with oligoasthenozoospermia

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21 January 2018

Identifiers

DOI

10.1186/1471-2350-13-69

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Europe PubMed Central

PubMed publication ID

22876777

retrieved

1 August 2017

PMC publication ID

3495047

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22876777

retrieved

1 August 2017

PubMed publication ID

22876777

1 reference

stated in

Europe PubMed Central

PubMed publication ID

22876777

retrieved

1 August 2017

ResearchGate publication ID

230643874

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