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Updated: Jun 5, 2025

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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Non-expressing homozygous C282Y carriers and haemochromatosis
1Department of Medicine, Western University, London, ON, Canada.
Abstract
No abstract available in PubMed .
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