LRRK2: bridging the gap between sporadic and hereditary Parkinson's disease
Author:
Publisher
Elsevier BV
Subject
Clinical Neurology
Reference9 articles.
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2. LRRK2 Gly2019Ser penetrance in Arab–Berber patients from Tunisia: a case-control genetic screen;Hulihan;Lancet Neurol,2008
3. Prevalence of the LRRK2 G2019S mutation in a UK community-based idiopathic Parkinson's disease cohort;Williams-Gray;J Neurol Neurosurg Psychiatry,2006
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1. The Role of Genetics in Alzheimer's Disease and Parkinson's Disease;Neurodegeneration and Alzheimer's Disease;2019-05-11
2. Penetrance of LRRK2 G2385R and R1628P is modified by common PD-associated genetic variants;Parkinsonism & Related Disorders;2012-09
3. Mitochondrial complex I inhibitor rotenone-induced toxicity and its potential mechanisms in Parkinson’s disease models;Critical Reviews in Toxicology;2012-05-11
4. Measuring the Activity of Leucine-Rich Repeat Kinase 2: A Kinase Involved in Parkinson’s Disease;Methods in Molecular Biology;2011-08-25
5. A QUICK Screen for Lrrk2 Interaction Partners – Leucine-rich Repeat Kinase 2 is Involved in Actin Cytoskeleton Dynamics;Molecular & Cellular Proteomics;2011-01
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