Article
Comprehensive evaluation of common genetic variation within LRRK2 reveals evidence for association with sporadic Parkinson's disease.
Human molecular genetics - 1 Dec 2005
Skipper Lisa, Li Yi, Bonnard Carine, Pavanni Ratnagopal, Yih Yuen, Chua Eva, Sung Wing-Kin, Tan Louis, Wong Meng-Cheong, Tan Eng-King, Liu Jianjun
Abstract excerpt
Parkinson's disease (PD) is a complex neurodegenerative disorder whose aetiologies are largely unknown. To date, mutations in six genes have been found causal for some rare familial forms of the disease and common variation within at least three of these is associated with the more common sporadi...
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