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Updated: Jun 15, 2025

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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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Reassessing the unifying hypothesis for hypercontractility caused by myosin mutations in hypertrophic cardiomyopathy
James A Spudich1, Neha Nandwani2, Julien Robert-Paganin3
1Department of Biochemistry, Stanford University School of Medicine, Stanford, CA, 94305, USA. jspudich@stanford.edu.
The EMBO Journal
|August 27, 2024
Abstract
No abstract available in PubMed .
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