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Updated: Jun 1, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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RBM20 Gene in Patients With Cardiomyopathy: Phenotypic Expression for Loss-of-Function Versus Hotspot Variants

Alexis Hermida1,2,3,4, Flavie Ader5,6,7, Gilles Millat8

  • 1Cardiology, Arrhythmia, and Cardiac Stimulation Service, Amiens-Picardie University Hospital, Amiens, France (A.H., L.V., F.F., C.B.).

Circulation. Heart Failure
|January 17, 2025
PubMed
Abstract

No abstract available in PubMed .

Keywords:
cardiomyopathydilated

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