Allelic heterogeneity of Crigler-Najjar type I syndrome: a study of 24 cases

Clin Genet. 2004 Dec;66(6):571-2. doi: 10.1111/j.1399-0004.2004.00371.x.
No abstract available

Publication types

  • Letter

MeSH terms

  • Crigler-Najjar Syndrome / genetics*
  • Glucuronosyltransferase / genetics
  • Humans
  • Hyperbilirubinemia, Hereditary / genetics*
  • Infant, Newborn
  • Mutation

Substances

  • UGT1A1 enzyme
  • Glucuronosyltransferase