Brain stem lesion in mitochondrial DNA G11778A mutation of Leber's hereditary optic neuropathy

J Formos Med Assoc. 2015 Jul;114(7):668-9. doi: 10.1016/j.jfma.2014.01.005. Epub 2014 Feb 20.
No abstract available

Publication types

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

MeSH terms

  • Adult
  • Brain Stem / physiopathology*
  • DNA, Mitochondrial / genetics*
  • Humans
  • Magnetic Resonance Imaging
  • Male
  • Mutation
  • Optic Atrophy, Hereditary, Leber / genetics*

Substances

  • DNA, Mitochondrial