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Updated: May 25, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Mitochondrial A3243G mutation with manifestation of acute dilated cardiomyopathy
Nicolas Stalder1, Nuray Yarol, Piergiorgio Tozzi
1Service de Cardiologie, Centre Hospitalier Universitaire Vaudois, Faculté Biologie et Médecine, Université de Lausanne, Lausanne, Switzerland.
No abstract available in PubMed .
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