Optic atrophy and negative electroretinogram in a patient associated with a novel OPA1 mutation

Graefes Arch Clin Exp Ophthalmol. 2006 Feb;244(2):274-5. doi: 10.1007/s00417-005-0050-3. Epub 2005 Jul 15.
No abstract available

Publication types

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

MeSH terms

  • Electroretinography*
  • Female
  • GTP Phosphohydrolases / genetics*
  • Humans
  • Male
  • Middle Aged
  • Mutation*
  • Optic Atrophy, Autosomal Dominant / genetics*

Substances

  • GTP Phosphohydrolases
  • OPA1 protein, human