A homozygous mutation in a Chinese man with Crigler–Najjar syndrome type II and a family genetic analysis
Author:
Publisher
Wiley
Subject
Gastroenterology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1751-2980.2008.00328.x/fullpdf
Reference17 articles.
1. A Neurophysiological Study in Children and Adolescents with Crigler-Najjar Syndrome Type I
2. Phenobarbital Following Phototherapy for Crigler-Najjar Syndrome Type II with Good Fetal Outcome: A Case Report
3. Hematologically important mutations: Bilirubin UDP-glucuronosyltransferase gene mutations in Gilbert and Crigler–Najjar syndromes
Cited by 2 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Spectrum of UGT1A1 Variations in Chinese Patients with Crigler-Najjar Syndrome Type II;PLOS ONE;2015-05-20
2. Crigler-Najjar syndrome type II in a Chinese boy resulting from three mutations in the bilirubin uridine 5′-diphosphate-glucuronosyltransferase (UGT1A1) gene and a family genetic analysis;BMC Pediatrics;2014-10-15
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