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...

Descripció completa

Guardat en:
Dades bibliogràfiques
Autors principals: 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
Format: Artigo
Idioma:Inglês
Publicat: 2007
Matèries:
Article
Accés en línia: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
Etiquetes: Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!

Ítems similars