Unusual features of mitochondrial degeneration in skeletal muscle of patients with nuclear complex I mutation

Acta Neuropathol. 2005 Aug;110(2):199-202. doi: 10.1007/s00401-005-1036-2. Epub 2005 Jun 25.
No abstract available

Publication types

  • Letter

MeSH terms

  • Electron Transport Complex I / genetics*
  • Humans
  • Infant
  • Infant, Newborn
  • Male
  • Microscopy, Electron, Transmission
  • Mitochondria, Muscle / metabolism
  • Mitochondria, Muscle / pathology*
  • Mitochondrial Diseases / genetics
  • Mitochondrial Diseases / metabolism
  • Mitochondrial Diseases / pathology*
  • Muscle, Skeletal / metabolism
  • Muscle, Skeletal / pathology*
  • Muscle, Skeletal / ultrastructure
  • Mutation
  • NADH Dehydrogenase

Substances

  • NDUFS1 protein, human
  • NADH Dehydrogenase
  • Electron Transport Complex I