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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model

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An autopsy case of Fabry's disease with cardiac manifestations

Osamu Suzuki1, Masafumi Abe

  • 1First Department of Pathology, School of Medicine, Fukushima Medical University, Hikarigaoka, Fukushima, Japan. osuzuki@fmu.ac.jp

Journal of Clinical and Experimental Hematopathology : JCEH
|November 13, 2009
PubMed

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