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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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A case report of mixed left ventricular non-compaction/hypertrophic cardiomyopathy phenotype in a child

Chiara Cirillo1, Emanuele Monda1, Santo Dellegrottaglie2

  • 1Department of Translational Medical Sciences, Inherited and Rare Cardiovascular Diseases, University of Campania 'Luigi Vanvitelli', Monaldi Hospital, Via Leonardo Bianchi, 80131 Naples, Italy.

European Heart Journal. Case Reports
|February 17, 2025
PubMed
Abstract

No abstract available in PubMed .

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