Founder mutations of CYP1B1 gene in patients with congenital glaucoma from the United States and Brazil

J Med Genet. 2004 Jan;41(1):e6. doi: 10.1136/jmg.2003.010777.
No abstract available

Publication types

  • Letter
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Age of Onset
  • Aryl Hydrocarbon Hydroxylases / genetics*
  • Brazil / epidemiology
  • Child, Preschool
  • Cytochrome P-450 CYP1B1
  • Female
  • Founder Effect*
  • Glaucoma / congenital*
  • Glaucoma / epidemiology
  • Glaucoma / genetics*
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Mutation / genetics*
  • United States / epidemiology

Substances

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