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Updated: Jun 1, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

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GATA4 specific nonsynonymous single-nucleotide polymorphisms in congenital heart disease patients of Mysore, India

Sosalagere M Dinesh1, Kusuma Lingaiah, Mysore R Savitha

  • 1Genomics Laboratory, Department of Studies in Zoology, University of Mysore, Mysore, India.

Genetic Testing and Molecular Biomarkers
|June 3, 2011
PubMed

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