Worldwide frequency of G2019S LRRK2 mutation in Parkinson's disease: A systematic review
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Geriatrics and Gerontology,Neurology
Reference90 articles.
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3. Mutations in LRRK2 cause autosomal dominant parkinsonism with pleomorphic pathology;Zimprich;Neuron,2004
4. A frequent LRRK2 gene mutation associated with autosomal dominant Parkinson's disease;Di Fonzo;Lancet,2005
5. Identification of a novel LRRK2 mutation linked to autosomal dominant parkinsonism: evidence of a common founder across European populations;Kachergus;Am J Hum Genet,2005
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