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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Identification by next-generation sequencing of 2 novel cases of noncompaction cardiomyopathy associated with 1p36

María Luisa Peña-Peña1, Juan Pablo Trujillo-Quintero2, Dolores García-Medina3

  • 1Servicio de Cardiología, Hospital Universitario Virgen del Rocío, Sevilla, Spain.

Revista Espanola De Cardiologia (English Ed.)
|March 21, 2020
PubMed
Abstract

No abstract available in PubMed .

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