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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Usefulness of genetic testing for hypertrophic cardiomyopathy in real-world practice

Marta Cobo-Marcos1, Sofía Cuenca1, Jose María Gámez Martínez2

  • 1Unidad de Insuficiencia Cardiaca y Miocardiopatías, Servicio de Cardiología, Hospital Universitario Puerta de Hierro, Majadahonda, Madrid, Spain.

Revista Espanola De Cardiologia (English Ed.)
|April 30, 2014
PubMed
Abstract

No abstract available in PubMed .

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