Familial dementia with Lewy bodies with VPS13C mutations

Parkinsonism Relat Disord. 2020 Dec:81:31-33. doi: 10.1016/j.parkreldis.2020.10.008. Epub 2020 Oct 7.
No abstract available

Publication types

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

MeSH terms

  • Codon, Nonsense
  • Female
  • Humans
  • Lewy Body Disease / genetics*
  • Middle Aged
  • Parkinsonian Disorders / genetics
  • Pedigree
  • Proteins / genetics*
  • Siblings

Substances

  • Codon, Nonsense
  • Proteins
  • VPS13C protein, human