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Updated: Apr 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

Published on: August 8, 2022

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Mavacamten in Obstructive Hypertrophic Cardiomyopathy and C282Y Homozygous Hereditary Hemochromatosis: A

Riya Sam1, Anil Ananthaneni2, Maria Isabel Planek1

  • 1Division of Cardiology, Endeavor Health, Glenview, Illinois, USA; Division of Cardiology, University of Chicago Pritzker School of Medicine, Chicago, Illinois, USA.

JACC. Case Reports
|March 31, 2026
PubMed
Abstract

Keywords:
cardiac myosin inhibitorshereditary hemochromatosishypertrophic cardiomyopathymavacamtenmultimodality imaging

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