Cerebellar ataxia as atypical manifestation of the 3243A>G MELAS mutation

Clin Genet. 2004 Jan;65(1):64-5. doi: 10.1111/j..2004.00185.x.
No abstract available

Publication types

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

MeSH terms

  • Brain / pathology
  • Cerebellar Ataxia / etiology*
  • Cerebellar Ataxia / genetics*
  • DNA, Mitochondrial / genetics
  • Humans
  • MELAS Syndrome / complications*
  • MELAS Syndrome / genetics*
  • Magnetic Resonance Imaging
  • Male
  • Middle Aged
  • Point Mutation
  • RNA, Transfer, Leu / genetics*

Substances

  • DNA, Mitochondrial
  • RNA, Transfer, Leu