Identification of Defect in the Genes for Bilirubin UDP-Glucuronosyltransferase in a Patient with Crigler-Najjar Syndrome Type II

Biochemical and Biophysical Research Communications - Tập 197 - Trang 1239-1244 - 1993
S. Aono1, Y. Yamada1, H. Keino1, N. Hanada1, T. Nakagawa1, Y. Sasaoka1, T. Yazawa1, H. Sato1, O. Koiwai1
1Aichi Prefectural Colony, Inst Dev Res, Dept Perinatol, Kasugai, Aichi 48003, Japan; Aichi Prefectural Colony, Inst Dev Res, Dept Genet, Kasugai, Aichi 48003, Japan; Hanada Childrens Clin, Okazaki, Aichi 44431, Japan; Shiga Univ Med Sci, Dept Biol, Otsu, Shiga 52021, Japan and Aichi Canc Ctr, Res Inst, Dept Biochem, Nagoya, Aichi 464, Japan

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Biochemical and Biophysical Research Communications

Tập 197

1239-1244

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