Familial genes in sporadic disease: Common variants of α-Synuclein gene associate with Parkinson’s disease

Genetic variation of the α-synuclein gene (SNCA) is known to cause familial parkinsonism, however the role of SNCA variants in sporadic Parkinson’s disease (PD) remains elusive. The present study identifies an association of common SNCA polymorphisms with disease susceptibility in a series of Irish...

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Detalhes bibliográficos
Main Authors: Ross, Owen A., Gosal, David, Stone, Jeremy T., Lincoln, Sarah J., Heckman, Michael G., Irvine, Brent G., Johnston, Janet A., Gibson, J. Mark, Farrer, Matthew J., Lynch, Timothy
Formato: Artigo
Idioma:Inglês
Publicado em: 2007
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC2970620/
https://ncbi.nlm.nih.gov/pubmed/17531291
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mad.2007.04.002
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