Optic mitochondriopathies

Neurology. 2005 Mar 22;64(6):940-1. doi: 10.1212/01.WNL.0000157285.93611.B2.
No abstract available

Publication types

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

MeSH terms

  • Apoptosis / genetics
  • DNA, Mitochondrial / metabolism
  • Electron Transport / genetics
  • GTP Phosphohydrolases / genetics*
  • Genetic Predisposition to Disease / genetics
  • Humans
  • Mitochondria / genetics
  • Mitochondria / metabolism*
  • Mutation / genetics
  • Nerve Degeneration / genetics
  • Nerve Degeneration / metabolism*
  • Nerve Degeneration / physiopathology
  • Optic Atrophy, Autosomal Dominant / genetics*
  • Optic Atrophy, Autosomal Dominant / metabolism*
  • Optic Atrophy, Autosomal Dominant / physiopathology
  • Optic Nerve / metabolism*
  • Optic Nerve / pathology
  • Optic Nerve / physiopathology

Substances

  • DNA, Mitochondrial
  • GTP Phosphohydrolases
  • OPA1 protein, human