SNCA Variants Are Associated with Increased Risk for Multiple System Atrophy

To test whether the synucleinopathies Parkinson’s disease and multiple system atrophy (MSA) share a common genetic etiology, we performed a candidate single nucleotide polymorphism (SNP) association study of the 384 most associated SNPs in a genome-wide association study of Parkinson’s disease in 41...

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Detalhes bibliográficos
Main Authors: Scholz, Sonja W., Houlden, Henry, Schulte, Claudia, Sharma, Manu, Li, Abi, Berg, Daniela, Melchers, Anna, Paudel, Reema, Gibbs, J. Raphael, Simon-Sanchez, Javier, Paisan-Ruiz, Coro, Bras, Jose, Ding, Jinhui, Chen, Honglei, Traynor, Bryan J., Arepalli, Sampath, Zonozi, Ryan R., Revesz, Tamas, Holton, Janice, Wood, Nick, Lees, Andrew, Oertel, Wolfgang, Wüllner, Ullrich, Goldwurm, Stefano, Pellecchia, Maria Teresa, Illig, Thomas, Riess, Olaf, Fernandez, Hubert H., Rodriguez, Ramon L., Okun, Michael S., Poewe, Werner, Wenning, Gregor K., Hardy, John A., Singleton, Andrew B., Gasser, Thomas
Formato: Artigo
Idioma:Inglês
Publicado em: 2009
Assuntos:
Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3520128/
https://ncbi.nlm.nih.gov/pubmed/19475667
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/ana.21685
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