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Updated: Dec 8, 2025

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Assessing Prevalence and Characteristics of Rare Disease Cardiomyopathies: A Modest Proposal
1Cardiovascular Medicine Group, Covance Inc., Princeton, NJ.
No abstract available in PubMed .
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