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Updated: Jun 5, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Navigating The Complex Path From Monogenic to Polygenic Clinical Genetic Testing in Hypertrophic Cardiomyopathy

Roddy Walsh1

  • 1Department of Experimental Cardiology, Amsterdam University Medical Centre, University of Amsterdam, Amsterdam, the Netherlands; Cardiovascular and Genomics Research Institute, City St. George's University of London, London, United Kingdom.

JACC. Heart Failure
|December 4, 2024
PubMed
Summary

No abstract available in PubMed .

Keywords:
HCMgenetic modifiershypertrophic cardiomyopathyrisk factors

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