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Updated: Apr 15, 2026

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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Compound heterozygous C282Y/Q283P and Q283P/H63D mutations in haemochromatosis
Adriaan van Gammeren1, Ellen de Baar2, Lianne Schrauwen2
1Department of Clinical Chemistry and Haematology, Breda, the Netherlands. avangammeren@amphia.nl.
British Journal of Haematology
|April 9, 2015
Abstract
No abstract available in PubMed .
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