Revisiting the issue of mitochondrial DNA content in optic mitochondriopathies

Neurology. 2012 Oct 2;79(14):1517-9. doi: 10.1212/WNL.0b013e31826d5f72. Epub 2012 Sep 19.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Blood Cells / pathology
  • Case-Control Studies
  • Cohort Studies
  • DNA, Mitochondrial / genetics*
  • Family Health*
  • Female
  • GTP Phosphohydrolases / genetics*
  • Humans
  • Italy
  • Male
  • Mitochondrial Diseases / complications
  • Mitochondrial Diseases / genetics*
  • Mitochondrial Diseases / pathology
  • Muscle, Skeletal / pathology
  • Mutation / genetics*
  • Optic Atrophy, Hereditary, Leber / complications
  • Optic Atrophy, Hereditary, Leber / genetics*
  • Optic Atrophy, Hereditary, Leber / pathology
  • Optic Nerve / pathology

Substances

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