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Updated: Aug 9, 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

Published on: August 8, 2022

Infantile restrictive cardiomyopathy resulting from a mutation in the cardiac troponin T gene

Stacie B Peddy1, Luca A Vricella, Jane E Crosson

  • 1Department of Pediatric Cardiology, Johns Hopkins University School of Medicine, Baltimore, MD 21287, USA.

Pediatrics
|May 3, 2006
PubMed

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