Adult-onset myoclonus ataxia associated with the mitochondrial m.8993T>C "NARP" mutation

Mov Disord. 2015 Sep;30(10):1432-3. doi: 10.1002/mds.26358. Epub 2015 Aug 12.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Aged
  • DNA, Mitochondrial / genetics*
  • Humans
  • Male
  • Mutation
  • Myoclonic Cerebellar Dyssynergia / genetics*

Substances

  • DNA, Mitochondrial

Supplementary concepts

  • Hunt's syndrome