SAKIYAMA Y. | Department of Human Gene Therapy, Hokkaido University Graduate School of Medicine

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著作論文

A Novel Missense Mutation (p.P52R) in Amelogenin Gene Causing X-linked Amelogenesis Imperfecta
The first report of a novel mutation in the amelogenin gene in a Japanese family affected with X-linked amelogenesis imperfecta (Oral Session)(Japanese Teratology Society 43rd Annual Meeting)
Identification of a novel mutation in the enamelin gene in a Japanese family affected with autosomal dominant amelogenesis imperfecta(Oral Session)(Japanese Teratology Society 43rd Annual Meeting)
Autosomal-dominant Hypoplastic Form of Amelogenesis Imperfecta Caused by an Enamelin Gene Mutation at the Exon-Intron Boundary

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