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Updated: Nov 15, 2025

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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Editorial for Special Issue "Genetic Basis and Epidemiology of Myopathies"

Eleni Peristeri1, Efthimios Dardiotis1

  • 1Department of Neurology, Faculty of Medicine, University of Thessaly, 41100 Larissa, Greece.

International Journal of Molecular Sciences
|March 6, 2021
PubMed

Keywords:
epidemiologygenetic basismyopathies

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