Gene symbol: CYP1B1. Disease: Primary congenital glaucoma. Accession #Hm0544

Hum Genet. 2006 Feb;118(6):779.
No abstract available

MeSH terms

  • Amino Acid Substitution
  • Aryl Hydrocarbon Hydroxylases / genetics*
  • Cytochrome P-450 CYP1B1
  • Glaucoma / genetics*
  • Humans
  • Mutation, Missense

Substances

  • Aryl Hydrocarbon Hydroxylases
  • CYP1B1 protein, human
  • Cytochrome P-450 CYP1B1