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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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Ehlers-Danlos syndrome, vascular type: a novel missense mutation in the COL3A1 gene

Mitsuo Masuno1, Atsushi Watanabe, Banyar Than Naing

  • 1Department of Pediatrics,Kawasaki Medical School, Kurashiki, Japan. m-masuno@mw.kawasaki-m.ac.jp

Congenital Anomalies
|November 28, 2012
PubMed

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