SNCA and MAPT genes: Independent and joint effects in Parkinson disease in the Italian population

BACKGROUND: Significant efforts have been focused on investigating the contribution of common variants to Parkinson disease (PD) risk. Several independent GWAS and metanalysis studies have shown a genome-wide significant association of single nucleotide polymorphisms (SNPs) in the α-synuclein (SNCA)...

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Detalles Bibliográficos
Autores principales: Trotta, Luca, Guella, Ilaria, Soldà, Giulia, Sironi, Francesca, Tesei, Silvana, Canesi, Margherita, Pezzoli, Gianni, Goldwurm, Stefano, Duga, Stefano, Asselta, Rosanna
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Science 2012
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314966/
https://www.ncbi.nlm.nih.gov/pubmed/22104010
http://dx.doi.org/10.1016/j.parkreldis.2011.10.014

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3314966/
https://www.ncbi.nlm.nih.gov/pubmed/22104010
http://dx.doi.org/10.1016/j.parkreldis.2011.10.014

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