Genetic Analysis of Synphilin-1 in Familial Parkinson's Disease-Reference-Cited by-同舟云学术

Genetic Analysis of Synphilin-1 in Familial Parkinson's Disease

Published:2001-04 Issue:2 Volume:8 Page:317-323
ISSN:0969-9961
Container-title:Neurobiology of Disease
language:en
Short-container-title:Neurobiology of Disease

Author:

Farrer M.,Destée A.,Levecque C.,Singleton A.,Engelender S.,Becquet E.,Mouroux V.,Richard F.,Defebvre L.,Crook R.,Hernandez D.,Ross C.A.,Hardy J.,Amouyel P.,Chartier-Harlin M-C.

Publisher

Elsevier BV

Subject

Neurology

Reference19 articles.

1. Prevalence of parkinsonism and Parkinson's disease in Europe: The Europarkinson Collaborative Study. European Community Concerted Action on the Epidemiology of Parkinson's Disease;de Rijk;J. Neurol. Neurosurg. Psychiatry,1997

2. Synphilin-1 associates with α-synuclein and promotes the formation of cytosolic inclusions;Engelender;Nat. Genet.,1999

3. The α-synuclein-associated protein, synphilin-1, gene structure and localization and presence of synphilin-1 protein in Lewy bodies;Engelender;Am. J. Hum. Genet.,1999

4. A chromosome 4p haplotype segregating with Parkinson's disease and postural tremor;Farrer;Hum. Mol. Genet.,1999

5. Genetic heterogeneity in familial Parkinson's disease;Farrer,1999

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