Rare homozygous PRKN exon 8 and 9 deletion in Malay familial early-onset Parkinson's disease

Ann Acad Med Singap. 2021 Apr;50(4):353-355. doi: 10.47102/annals-acadmedsg.2020508.
No abstract available

Publication types

  • Letter

MeSH terms

  • Age of Onset
  • Exons / genetics
  • Humans
  • Malaysia / epidemiology
  • Mutation
  • Parkinson Disease* / genetics