A novel rare variant of LRRK2 associated with familial Parkinson's disease: p.R1501W

Parkinsonism Relat Disord. 2020 Jul:76:46-48. doi: 10.1016/j.parkreldis.2020.05.035. Epub 2020 Jun 2.
No abstract available

Keywords: Familial Parkinson's disease; Genetics; LRRK2.

Publication types

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

MeSH terms

  • Age of Onset
  • Aged
  • Aged, 80 and over
  • Disease Progression
  • Female
  • Humans
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2 / genetics*
  • Male
  • Parkinson Disease / genetics*
  • Parkinson Disease / physiopathology*
  • Pedigree

Substances

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