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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
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Sudden Death in Hypertrophic Cardiomyopathy Is Rare
1Royal Papworth Hospital Foundation Trust, Cambridge Biomedical Campus, UK. Department of Biochemistry, University of Cambridge, UK.
Circulation
|November 19, 2019
Abstract
No abstract available in PubMed .
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