Complex I respiratory defect in LHON plus dystonia with no mitochondrial DNA mutation

Br J Ophthalmol. 2005 Oct;89(10):1380-1. doi: 10.1136/bjo.2005.072819.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adolescent
  • DNA, Mitochondrial / genetics*
  • Dystonic Disorders / genetics*
  • Electron Transport Complex I / genetics*
  • Female
  • Humans
  • Mutation*
  • Optic Atrophy, Hereditary, Leber / genetics*

Substances

  • DNA, Mitochondrial
  • Electron Transport Complex I