articleTop 1% cited
A novel α-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson's disease-type pathology
Neurobiology of Aging · 2014 · Vol. 35(9) · pp. 2180.e1–2180.e5
Petra Pasanen(University of Turku)Liisa Myllykangas✉(University of Helsinki)Maija Siitonen(University of Turku)Anna Raunio(University of Helsinki)Seppo Kaakkola(Helsinki University Hospital)Jukka Lyytinen(University of Helsinki)Pentti J. Tienari(University of Helsinki)Minna Pöyhönen(University of Helsinki)Anders Paetau(University of Helsinki)
Parkinson's Disease Mechanisms and TreatmentsBotulinum Toxin and Related Neurological DisordersNeurological diseases and metabolismPathologyParkinsonismAtrophyLocus coeruleusGliosisSubstantia nigraAlpha-synucleinDentate gyrusMedicineParkinson's disease
MeSH terms
AdultBrainDNA-Binding ProteinsFemaleHumansMiddle AgedMutationParkinson DiseasePedigreePhenotypeSpinal CordNeuritesMultiple System Atrophyalpha-SynucleinGenetic Association Studies
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References
AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's disease
Nature Genetics · 1998 · 3,865 citations
Alpha‐synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease
Movement Disorders · 2013 · 654 citations
Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease
Science · 1997 · 8,181 citations
Second consensus statement on the diagnosis of multiple system atrophy
Neurology · 2008 · 3,118 citations
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