Associated Papers
Splicing: is there an alternative contribution to Parkinson's disease?
La Cognata V et al.
Neurogenetics, 2015
Genetic etiology of Parkinson disease associated with mutations in the SNCA, PARK2, PINK1, PARK7, and LRRK2 genes: a mutation update.
Nuytemans K et al.
Human Mutation, 2010
20506312 (PubMed )
Supplement: humu0031-0763-SD1.pdf
LRRK2 screening in a Canadian Parkinson's disease cohort.
Grimes DA et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques, 2007
Comprehensive analysis of the LRRK2 gene in sixty families with Parkinson's disease.
Di Fonzo A et al.
European Journal of Human Genetics : Ejhg, 2006
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