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Updated: May 24, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
03:45

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

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Next-generation sequencing to identify genetic causes of cardiomyopathies

Nadine Norton1, Duanxiang Li, Ray E Hershberger

  • 1Cardiovascular Division, Department of Medicine, University of Miami Miller School of Medicine, Miami, Florida 33136, USA.

Current Opinion in Cardiology
|March 17, 2012
PubMed
Abstract

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