Association of LRRK2 and GBA mutations in a Brazilian family with Parkinson's disease

Parkinsonism Relat Disord. 2015 Jul;21(7):825-6. doi: 10.1016/j.parkreldis.2015.03.029. Epub 2015 May 2.
No abstract available

Keywords: G2019S; GBA; Genetics; L444P; LRRK2; Parkinson's disease.

Publication types

  • Case Reports
  • Letter

MeSH terms

  • Brazil
  • Female
  • Genetic Association Studies*
  • Glucosylceramidase / genetics*
  • Humans
  • Leucine-Rich Repeat Serine-Threonine Protein Kinase-2
  • Middle Aged
  • Mutation / genetics*
  • Parkinson Disease / diagnosis*
  • Parkinson Disease / genetics*
  • Pedigree
  • Protein Serine-Threonine Kinases / genetics*

Substances

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