Parkinson's disease in GTP cyclohydrolase 1 mutation carriers
ContributorsInternational Parkinson's Disease Genomics Consortium; UCL-exomes consortium
CollaboratorsKrack, Paul
Published inBrain, vol. 137, no. Pt 9, p. 2480-2492
Publication date2014
Keywords
- Adolescent
- Adult
- Aged
- Aged, 80 and over
- Child
- Databases, Genetic
- Europe/epidemiology
- Female
- GTP Cyclohydrolase/*genetics
- Genetic Variation
- Humans
- Male
- Middle Aged
- Mutation/*genetics
- Parkinson Disease/*diagnosis/epidemiology/*genetics
- Pedigree
- Risk
- United States/epidemiology
- Young Adult
- DOPA-responsive-dystonia
- Gch1
- Parkinson's disease
- *Heterozygote
- dopamine
- exome sequencing
Research group
Citation (ISO format)
International Parkinson’s Disease Genomics Consortium, UCL-exomes consortium. Parkinson’s disease in GTP cyclohydrolase 1 mutation carriers. In: Brain, 2014, vol. 137, n° Pt 9, p. 2480–2492. doi: 10.1093/brain/awu179
Main files (1)
Article (Published version)
Identifiers
- PID : unige:95946
- DOI : 10.1093/brain/awu179
- PMID : 24993959
ISSN of the journal0006-8950
