Associated Papers
A genetic analysis of a Spanish population with early onset Parkinson's disease.
Cristina TP et al.
Plos One, 2020
Splicing: is there an alternative contribution to Parkinson's disease?
La Cognata V et al.
Neurogenetics, 2015
Identification of novel variants in LRRK2 gene in patients with Parkinson's disease in Serbian population.
Janković MZ et al.
Journal of the Neurological Sciences, 2015
Identification of three novel LRRK2 mutations associated with Parkinson's disease in a Calabrian population.
Anfossi M et al.
Journal of Alzheimer's Disease : Jad, 2014
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
Identification of four novel potentially Parkinson's disease associated LRRK2 variations among Iranian patients.
Shojaee S et al.
Neuroscience Letters, 2009
A clinic-based screening of mutations in exons 31, 34, 35, 41, and 48 of LRRK2 in Iranian Parkinson's disease patients.
Shojaee S et al.
Movement Disorders : Official Journal of the Movement Disorder Society, 2009
LRRK2 and Parkinson's disease in Norway.
Toft M et al.
Acta Neurologica Scandinavica. Supplementum, 2007
The LRRK2 I2012T, G2019S and I2020T mutations are not common in patients with essential tremor.
Deng H et al.
Neuroscience Letters, 2006
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
Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease.
Skipper L et al.
Human Molecular Genetics, 2005
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