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Updated: Jan 22, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Compound sarcomeric mutations causing hypertrophic cardiomyopathy in a young Sardinian soccer player: a family affair
Nicola Marziliano1,2,3,4, Valeria Orrù5, Tanuccia Secci5
1Department of Medicine and Health Sciences, University of Molise, Campobasso, Italy.
No abstract available in PubMed .
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