Familial ataxia, tremor, and dementia in a polish family with a novel mutation in the CCDC88C gene

Mov Disord. 2019 Jan;34(1):142-144. doi: 10.1002/mds.27536. Epub 2018 Nov 6.
No abstract available

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Ataxia / diagnosis
  • Ataxia / genetics
  • Dementia / diagnosis
  • Dementia / genetics*
  • Female
  • Humans
  • Intracellular Signaling Peptides and Proteins / genetics*
  • Male
  • Microfilament Proteins / genetics*
  • Middle Aged
  • Mutation / genetics*
  • Pedigree
  • Poland
  • Tremor / diagnosis
  • Tremor / genetics*

Substances

  • CCDC88C protein, human
  • Intracellular Signaling Peptides and Proteins
  • Microfilament Proteins