The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference16 articles.
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2. Italian Parkinson Genetics Network, A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease;Di Fonzo;Lancet,2005
3. A common LRRK2 mutation in idiopathic Parkinson's disease;Gilks;Lancet,2005
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