Coding variation in GBA explains the majority of the SYT11-GBA Parkinson's disease GWAS locus

Mov Disord. 2018 Nov;33(11):1821-1823. doi: 10.1002/mds.103. Epub 2018 Oct 9.
No abstract available

Keywords: GBA; Parkinson's disease; genome-wide association; glucocerebrosidase; risk allele.

Publication types

  • Letter
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Female
  • Genome-Wide Association Study
  • Glucosylceramidase / genetics*
  • Humans
  • Male
  • Mutation / genetics*
  • Parkinson Disease / genetics*
  • Synaptotagmins / genetics*

Substances

  • SYT11 protein, human
  • Synaptotagmins
  • Glucosylceramidase