LRRK2 R1441C mutation causing Parkinson's Disease in an Egyptian family

Neurol Neurochir Pol. 2022;56(2):191-192. doi: 10.5603/PJNNS.a2022.0008. Epub 2022 Jan 14.
No abstract available

Keywords: Egyptian; Parkinson’s Disease; R1441C mutation; leucine-rich repeat kinase 2 gene.

MeSH terms

  • Egypt
  • Humans
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2* / genetics
  • Mutation
  • Parkinson Disease* / genetics

Substances

  • LRRK2 protein, human
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2