UCL logo

UCL Discovery

UCL home » Library Services » Electronic resources » UCL Discovery

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.

Full text not available from this repository.
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
UCL classification: UCL > Provost and Vice Provost Offices
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology
UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Brain Sciences > UCL Queen Square Institute of Neurology > Department of Neuromuscular Diseases
URI: http://discovery.ucl.ac.uk/id/eprint/1510774
Downloads since deposit
0Downloads
Download activity - last month
Download activity - last 12 months
Downloads by country - last 12 months

Archive Staff Only

View Item View Item