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Updated: Oct 23, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Filamin C missense variant associated with severe right atrial disease and skeletal myopathy

Giulio Conte1, Flavia Piciacchia1, Argelia Medeiros-Domingo2

  • 1Istituto Cardiocentro Ticino, Ente Ospedaliero Cantonale, Lugano, Switzerland.

Journal of Cardiovascular Electrophysiology
|August 19, 2021
PubMed
Abstract

Keywords:
atrialcardiomyopathyfilamingeneticshigh-density mappingmyopathyvariants

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