Genetic heterogeneity for autosomal dominant familial hypertrophic cardiomyopathy in a Pakistani family.

Abstract excerpt

OBJECTIVE: To identify the gene causing inherited hypertrophic cardiomyopathy (HCM) in a Pakistani family. STUDY DESIGN: Cross-sectional, observational study. PLACE AND DURATION OF STUDY: Department of Cardiology, Shifa International Hospital and Biomedical and Genetic Engineering Laboratories, Islamabad, from 2005 to 2007. METHODOLOGY: A large family of 17 individuals was included in this study. In the family 6...

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• Share to Cardiomyopathy, Hypertrophic, Familial
• Share to Chromosomes, Human, Pair 1