A genome-wide association study in multiple system atrophy

OBJECTIVE: To identify genetic variants that play a role in the pathogenesis of multiple system atrophy (MSA), we undertook a genome-wide association study (GWAS). METHODS: We performed a GWAS with >5 million genotyped and imputed single nucleotide polymorphisms (SNPs) in 918 patients with MSA of...

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Detalles Bibliográficos
Autores principales: Sailer, Anna, Scholz, Sonja W., Nalls, Michael A., Schulte, Claudia, Federoff, Monica, Price, T. Ryan, Lees, Andrew, Ross, Owen A., Dickson, Dennis W., Mok, Kin, Mencacci, Niccolo E., Schottlaender, Lucia, Chelban, Viorica, Ling, Helen, O'Sullivan, Sean S., Wood, Nicholas W., Traynor, Bryan J., Ferrucci, Luigi, Federoff, Howard J., Mhyre, Timothy R., Morris, Huw R., Deuschl, Günther, Quinn, Niall, Widner, Hakan, Albanese, Alberto, Infante, Jon, Bhatia, Kailash P., Poewe, Werner, Oertel, Wolfgang, Höglinger, Günter U., Wüllner, Ullrich, Goldwurm, Stefano, Pellecchia, Maria Teresa, Ferreira, Joaquim, Tolosa, Eduardo, Bloem, Bastiaan R., Rascol, Olivier, Meissner, Wassilios G., Hardy, John A., Revesz, Tamas, Holton, Janice L., Gasser, Thomas, Wenning, Gregor K., Singleton, Andrew B., Houlden, Henry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2016
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5067544/
https://www.ncbi.nlm.nih.gov/pubmed/27629089
http://dx.doi.org/10.1212/WNL.0000000000003221

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