A third locus for dominant optic atrophy on chromosome 22q

J Med Genet. 2005 Jan;42(1):e1. doi: 10.1136/jmg.2004.025502.
No abstract available

Publication types

  • Letter
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chromosome Mapping
  • Chromosomes, Human, Pair 22*
  • Chromosomes, Human, Pair 3*
  • Denmark / epidemiology
  • Family
  • Female
  • France / epidemiology
  • GTP Phosphohydrolases / genetics*
  • Humans
  • Male
  • Mutation
  • Optic Atrophy, Autosomal Dominant / epidemiology
  • Optic Atrophy, Autosomal Dominant / genetics*
  • Prevalence

Substances

  • GTP Phosphohydrolases
  • OPA1 protein, human

Associated data

  • OMIM/165500
  • OMIM/300356
  • OMIM/535000
  • OMIM/60085
  • OMIM/600857
  • OMIM/605290
  • OMIM/605293
  • OMIM/606280