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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Publicado no:Neurology
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Lippincott Williams & Wilkins 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5067544/
https://ncbi.nlm.nih.gov/pubmed/27629089
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000003221
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