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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Genetic Dilated Cardiomyopathy: A Review
Madelyn Boslough1, Matthew R G Taylor1, Luisa Mestroni1
1University of Colorado Cardiovascular Institute and Adult Medical Genetics, Anschutz Medical Campus, Aurora, Colorado, US.
Abstract:
Dilated cardiomyopathy (DCM) is a leading cause of nonischemic heart failure. Genetic causes are identifiable in 25% to 30% of patients. This review describes the pathophysiology underlying genetic DCM, the genes most strongly associated with DCM, and both standard and novel therapies for treating genetic DCM.
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