Scientific article
Letter
English

Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson's disease

CollaboratorsPollak, Pierre
Published inJournal of medical genetics, vol. 46, no. 7, p. 458-464
Publication date2009
Abstract

Mutations in the leucine-rich-repeat kinase 2 (LRRK2) gene have been identified in families with autosomal dominant Parkinson's disease (ADPD), the most common of which is the p.G2019S substitution that has been found at varying frequencies worldwide. Because of the size of the LRRK2 gene, few studies have analysed the entire gene in large series of ADPD families.

Keywords
  • Adolescent
  • Adult
  • African Continental Ancestry Group/genetics
  • Aged
  • Aged, 80 and over
  • Analysis of Variance
  • Chi-Square Distribution
  • DNA Mutational Analysis/methods
  • European Continental Ancestry Group/genetics
  • Female
  • Gene Frequency
  • Humans
  • Male
  • Middle Aged
  • Mutation
  • Parkinsonian Disorders/diagnosis/genetics
  • Pedigree
  • Protein-Serine-Threonine Kinases/genetics
Citation (ISO format)
LESAGE, S et al. Molecular analyses of the LRRK2 gene in European and North African autosomal dominant Parkinson’s disease. In: Journal of medical genetics, 2009, vol. 46, n° 7, p. 458–464. doi: 10.1136/jmg.2008.062612
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Article (Published version)
accessLevelRestricted
Identifiers
Journal ISSN0022-2593
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