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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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Guidelines on the Diagnosis and Treatment of Hypertrophic Cardiomyopathy - 2024

Fabio Fernandes1, Marcus V Simões2, Edileide de Barros Correia3

  • 1Instituto do Coração (InCor) do Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo (HCFMUSP), São Paulo, SP - Brasil.

Arquivos Brasileiros De Cardiologia
|July 31, 2024
PubMed
Abstract

No abstract available in PubMed .

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