Movement Disorders (revue)

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Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease.

Identifieur interne : 000B09 ( Main/Exploration ); précédent : 000B08; suivant : 000B10

Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease.

Auteurs : Silke Appel-Cresswell [Canada] ; Carles Vilarino-Guell ; Mary Encarnacion ; Holly Sherman ; Irene Yu ; Brinda Shah ; David Weir ; Christina Thompson ; Chelsea Szu-Tu ; Joanne Trinh ; Jan O. Aasly ; Alex Rajput ; Ali H. Rajput ; A. Jon Stoessl ; Matthew J. Farrer

Source :

RBID : pubmed:23457019

English descriptors

Abstract

Alpha-synuclein plays a central role in the pathophysiology of Parkinson's disease. Three missense mutations in SNCA, the gene encoding alpha-synuclein, as well as genomic multiplications have been identified as causes for autosomal-dominantly inherited Parkinsonism.

DOI: 10.1002/mds.25421
PubMed: 23457019


Affiliations:


Links toward previous steps (curation, corpus...)


Le document en format XML

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<name sortKey="Appel Cresswell, Silke" sort="Appel Cresswell, Silke" uniqKey="Appel Cresswell S" first="Silke" last="Appel-Cresswell">Silke Appel-Cresswell</name>
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<nlm:affiliation>Department of Medicine (Neurology), Pacific Parkinson's Research Centre, University of British Columbia, Vancouver, British Columbia, Canada. silkec@mail.ubc.ca</nlm:affiliation>
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<wicri:regionArea>Department of Medicine (Neurology), Pacific Parkinson's Research Centre, University of British Columbia, Vancouver, British Columbia</wicri:regionArea>
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<div type="abstract" xml:lang="en">Alpha-synuclein plays a central role in the pathophysiology of Parkinson's disease. Three missense mutations in SNCA, the gene encoding alpha-synuclein, as well as genomic multiplications have been identified as causes for autosomal-dominantly inherited Parkinsonism.</div>
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