[The analysis of UGT1A1 gene mutations in hereditary unconjugated hyperbilirubinemia]

Zhonghua Gan Zang Bing Za Zhi. 2016 Nov 20;24(11):863-866. doi: 10.3760/cma.j.issn.1007-3418.2016.11.013.
[Article in Chinese]
No abstract available

MeSH terms

  • Bilirubin
  • Crigler-Najjar Syndrome* / genetics
  • Female
  • Gilbert Disease
  • Glucuronosyltransferase / genetics*
  • Humans
  • Male
  • Mutation*

Substances

  • UGT1A1 enzyme
  • Glucuronosyltransferase
  • Bilirubin