Maternally inherited diabetes and deafness with cerebellar ataxia: a new clinical phenotype associated with the mitochondrial DNA 3243 mutation

J Neurol. 1997 Jul;244(7):468-9. doi: 10.1007/s004150050126.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Adult
  • Brain / pathology
  • Cerebellar Ataxia / diagnosis
  • Cerebellar Ataxia / genetics*
  • DNA, Mitochondrial / genetics*
  • Deafness / genetics*
  • Diabetes Mellitus, Type 2 / genetics*
  • Humans
  • Japan
  • Magnetic Resonance Imaging
  • Male
  • Mutation*

Substances

  • DNA, Mitochondrial