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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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Novel cardiac myosin inhibitor for hypertrophic cardiomyopathy

Danuta Szczesna-Cordary1

  • 1Department of Molecular and Cellular Pharmacology, University of Miami, Miller School of Medicine, Miami, FL, USA.

The Journal of General Physiology
|August 13, 2024
PubMed
Abstract

No abstract available in PubMed .

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