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Updated: Jun 8, 2026

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

Published on: August 8, 2022

Congenital accessory mitral valve tissue anomaly in a patient with genetically confirmed hypertrophic cardiomyopathy

Beatrice Musumeci1, Paolo Spirito, Maria Isola Parodi

  • 1Divisione di Cardiologia, Azienda Ospedaliera Sant'Andrea, II Facoltà di Medicina, Università Sapienza, Rome, Italy.

Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography
|September 17, 2010
PubMed

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