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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Bibliografski detalji
Izdano u:Neurology
Glavni autori: 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
Format: Artigo
Jezik:Inglês
Izdano: Lippincott Williams & Wilkins 2016
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Article
Online pristup: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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