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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Fabry disease cardiomyopathy: from genes to clinical manifestations

Attila Béla Kertész1, István Édes

  • 1Nagyerdei krt 98, Debrecen, Hungary, H-4032. kertesz@dote.hu

Current Pharmaceutical Biotechnology
|January 28, 2012
PubMed

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