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Updated: May 10, 2025

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

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Publisher Correction: Extensive identification of genes involved in congenital and structural heart disorders and

Nadine Spielmann1, Gregor Miller1, Tudor I Oprea2,3,4

  • 1Institute of Experimental Genetics, German Mouse Clinic, Helmholtz Center Munich (GmbH), German Research Center for Environmental Health, Neuherberg, Germany.

Nature Cardiovascular Research
|April 23, 2025
PubMed
Abstract

No abstract available in PubMed .

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