LRRK2: Genetic mechanisms vs genetic subtypes
Author:
Funder
Aligning Science Across Parkinson’s
Publisher
Elsevier
Reference218 articles.
1. Clinical features of LRRK2-associated Parkinson's disease in central Norway;Aasly;Ann Neurol,2005
2. Higher frequency of certain cancers in LRRK2 G2019S mutation carriers with Parkinson disease: a pooled analysis;Agalliu;JAMA Neurol,2015
3. Parkinson disease phenotype in Ashkenazi Jews with and without LRRK2 G2019S mutations;Alcalay;Mov Disord,2013
4. Neuropsychological performance in LRRK2 G2019S carriers with Parkinson's disease;Alcalay;Parkinsonism Relat Disord,2015
5. Higher urine bis(monoacylglycerol)phosphate levels in LRRK2 G2019S mutation carriers: implications for therapeutic development;Alcalay;Mov Disord,2020
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