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Updated: Jun 13, 2026

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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Homozygotic intronic GAA mutation in three siblings with late-onset Pompe's disease

Anderson Kuntz Grzesiuk1, Sueli Mieko Oba Shinjo, Roseli da Silva

  • 1Hospital Santa Rosa, INEC, Cuiabá, MT, Brazil.

Arquivos De Neuro-Psiquiatria
|May 14, 2010
PubMed
Abstract

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