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Article

A low prevalence of MYH7/MYBPC3 mutations among familial hypertrophic cardiomyopathy patients in India.

Molecular and cellular biochemistry - 1 Jan 2012

Bashyam Murali D, Purushotham Guroji, Chaudhary Ajay K, Rao Katika Madhumohan, Acharya Vishal, Mohammad Tabrez A, Nagarajaram Hampapathalu A, Hariram Vuppaladadhiam, Narasimhan Calambur

Abstract excerpt

Familial Hypertrophic Cardiomyopathy (FHC) is an autosomal dominant disorder affecting the cardiac muscle and exhibits varied clinical symptoms because of genetic heterogeneity. Several disease causing genes have been identified and most code for sarcomere proteins. In the current study, we have carried out clinical and molecular analysis of FHC patients from India. FHC was detected using echocardiography and by...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 21959974
DOI: 10.1007/s11010-011-1077-x

Genes

MYH7
MYBPC3

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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