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Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
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FAM83H mutations in families with autosomal-dominant hypocalcified amelogenesis imperfecta

Jung-Wook Kim1, Sook-Kyung Lee, Zang Hee Lee

  • 1Department of Cell and Developmental Biology, Dental Research Institute, School of Dentistry, Seoul National University, 275-1 Yongon-dong, Chongno-gu, Seoul 110-768, Korea. pedoman@snu.ac.kr

American Journal of Human Genetics
|February 7, 2008
PubMed

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