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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Homozygous C677T mutation in the MTHFR gene as an independent risk factor for multiple small artery occlusions
Thrombosis Research
|March 26, 2004
Abstract
No abstract available in PubMed .
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