Cargando…
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)...
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: | |
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 |
Ejemplares similares
-
Glucocerebrosidase mutations in primary parkinsonism
por: Asselta, Rosanna, et al.
Publicado: (2014) -
DJ1 analysis in a large cohort of Italian early onset Parkinson Disease patients()
por: Sironi, Francesca, et al.
Publicado: (2013) -
LRRK2 mutations in Parkinson's disease: Confirmation of a gender effect in the Italian population
por: Cilia, Roberto, et al.
Publicado: (2014) -
SNCA Gene, but Not MAPT, Influences Onset Age of Parkinson's Disease in Chinese and Australians
por: Huang, Yue, et al.
Publicado: (2015) -
First Independent Replication of the Involvement of LARS2 in Perrault Syndrome by Whole-Exome Sequencing of an Italian Family
por: Soldà, Giulia, et al.
Publicado: (2015)