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A novel compound heterozygous variation of the uridine-diphosphoglucuronosyl transferase 1A1 gene that causes Crigler-Najjar syndrome type II.

Pharmacogenetics - 1 Oct 2001

Huang C S, Luo G A, Huang M J, Chen E S, Young T H, Chao Y C

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 11668224
DOI: 10.1097/00008571-200110000-00011

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A novel compound heterozygous variation of the uridine-diphosphoglucuronosyl transferase 1A1 gene that causes Crigler-Najjar syndrome type II.PMID 11668224Read ↗

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[A family study of the compound heterozygous mutation of the UGT1A1 gene causing Crigler-Najjar syndrome type II].Semantic proximity Read ↗

Gilbert and Crigler Najjar syndromes: an update of the UDP-glucuronosyltransferase 1A1 (UGT1A1) gene mutation database.Semantic proximity Read ↗

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