Biblio
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Analysis of common and rare variants in late-onset Parkinson disease. Neurol Genet. 2020;6(1):385.
. Common and rare GCH1 variants are associated with Parkinson's disease. Neurobiol Aging. 2019;73:231.e1-231.e6.
. SMPD1 mutations, activity, and α-synuclein accumulation in Parkinson's disease. Mov Disord. 2019;34(4):526-535.
. Genetic markers of Restless Legs Syndrome in Parkinson disease. Parkinsonism Relat Disord. 2015;21(6):582-5.
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