Lack of Association between TWNK Rare Variants and Parkinson's Disease in a Chinese Cohort

Mov Disord. 2023 Apr;38(4):708-709. doi: 10.1002/mds.29372.
No abstract available

Publication types

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

MeSH terms

  • DNA Helicases* / genetics
  • East Asian People
  • Genome-Wide Association Study
  • Humans
  • Mitochondrial Proteins* / genetics
  • Parkinson Disease* / epidemiology
  • Parkinson Disease* / genetics

Substances

  • TWNK protein, human
  • DNA Helicases
  • Mitochondrial Proteins