Crigler-Najjar type II syndrome may result from several types and combinations of mutations in the UGT1A1 gene

Clin Genet. 2006 Jun;69(6):525-7. doi: 10.1111/j.1399-0004.2006.00616.x.
No abstract available

Publication types

  • Letter

MeSH terms

  • Amino Acid Substitution / genetics
  • Child, Preschool
  • Crigler-Najjar Syndrome / classification
  • Crigler-Najjar Syndrome / genetics*
  • Genetic Heterogeneity*
  • Glucuronosyltransferase / genetics*
  • Humans
  • Infant
  • Mutation*
  • Point Mutation
  • Sequence Deletion

Substances

  • UGT1A1 enzyme
  • Glucuronosyltransferase