Genetic Modifiers of LRRK2 Parkinson's Disease: A Replication Study in Arab-Berbers

Mov Disord. 2024 Apr;39(4):751-753. doi: 10.1002/mds.29735. Epub 2024 Jan 31.
No abstract available

Publication types

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

MeSH terms

  • Aged
  • Arabs* / genetics
  • Female
  • Genetic Predisposition to Disease
  • Humans
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2* / genetics
  • Male
  • Middle Aged
  • Mutation
  • North African People*
  • Parkinson Disease* / genetics
  • Polymorphism, Single Nucleotide

Substances

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

Supplementary concepts

  • Berber people