Identification of Defect in the Genes for Bilirubin...

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

S. Aono, Y. Yamada, H. Keino, N. Hanada, T. Nakagawa, Y. Sasaoka, T. Yazawa, H. Sato, O. Koiwai
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Volume:
197
Year:
1993
Pages:
1245
DOI:
10.1006/bbrc.1993.2610
File:
PDF, 360 KB
1993
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