The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism
ContributorsKlebe, Stephan; Golmard, Jean-Louis; Nalls, Michael A; Saad, Mohamad; Singleton, Andrew B; Bras, Jose M; Hardy, John; Simon-Sanchez, Javier; Heutink, Peter; Kuhlenbäumer, Gregor; Charfi, Rim; Klein, Christine; Hagenah, Johann; Gasser, Thomas; Wurster, Isabel; Lesage, Suzanne; Lorenz, Delia; Deuschl, Günther; Durif, Franck; Pollak, Pierre; Damier, Philippe; Tison, François; Durr, Alexandra; Amouyel, Philippe; Lambert, Jean-Charles; Tzourio, Christophe; Maubaret, Cécilia; Charbonnier-Beaupel, Fanny; Tahiri, Khadija; Vidailhet, Marie; Martinez, Maria; Brice, Alexis; Corvol, Jean-Christophe
Published inJournal of neurology, neurosurgery and psychiatry, vol. 84, no. 6, p. 666-673
Publication date2013
Abstract
Keywords
- Age of Onset
- Aged
- Catechol O-Methyltransferase/genetics
- Genotype
- Humans
- Male
- Middle Aged
- Parkinson Disease/genetics
- Polymorphism, Single Nucleotide/genetics
- Sex Factors
Affiliation entities
Research groups
Citation (ISO format)
KLEBE, Stephan et al. The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson’s disease with a sexual dimorphism. In: Journal of neurology, neurosurgery and psychiatry, 2013, vol. 84, n° 6, p. 666–673. doi: 10.1136/jnnp-2012-304475
Main files (1)
Article (Published version)
Identifiers
- PID : unige:33603
- DOI : 10.1136/jnnp-2012-304475
- PMID : 23408064
Journal ISSN0022-3050