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LRRK2: Cause, Risk, and Mechanism

Paisan-Ruiz, C; Lewis, PA; Singleton, AB; (2013) LRRK2: Cause, Risk, and Mechanism. JOURNAL OF PARKINSONS DISEASE , 3 (2) pp. 85-103. 10.3233/JPD-130192.

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Type: Article
Title: LRRK2: Cause, Risk, and Mechanism
DOI: 10.3233/JPD-130192
Keywords: Science & Technology, Life Sciences & Biomedicine, Neurosciences, Neurosciences & Neurology, LRRK2, associated phenotype, disease risk, biology, future challenges, Parkinson's disease, parkinsonism, genetics, REPEAT KINASE 2, FAMILIAL PARKINSONS-DISEASE, AUTOSOMAL-DOMINANT PARKINSONISM, GENOME-WIDE ASSOCIATION, G2019S MUTATION CARRIERS, GENE LRRK2, CHINESE POPULATION, ALPHA-SYNUCLEIN, GTP-BINDING, ROC DOMAIN
URI: http://discovery.ucl.ac.uk/id/eprint/1510774
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