Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis

Multiple sclerosis (MS), a chronic disorder of the central nervous system and common cause of neurological disability in young adults, is characterized by moderate but complex risk heritability. Here we report the results of a genome-wide association study performed in a 1000 prospective case series...

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書誌詳細
出版年:Hum Mol Genet
主要な著者: Baranzini, Sergio E., Wang, Joanne, Gibson, Rachel A., Galwey, Nicholas, Naegelin, Yvonne, Barkhof, Frederik, Radue, Ernst-Wilhelm, Lindberg, Raija L.P., Uitdehaag, Bernard M.G., Johnson, Michael R., Angelakopoulou, Aspasia, Hall, Leslie, Richardson, Jill C., Prinjha, Rab K., Gass, Achim, Geurts, Jeroen J.G., Kragt, Jolijn, Sombekke, Madeleine, Vrenken, Hugo, Qualley, Pamela, Lincoln, Robin R., Gomez, Refujia, Caillier, Stacy J., George, Michaela F., Mousavi, Hourieh, Guerrero, Rosa, Okuda, Darin T., Cree, Bruce A. C., Green, Ari J., Waubant, Emmanuelle, Goodin, Douglas S., Pelletier, Daniel, Matthews, Paul M., Hauser, Stephen L., Kappos, Ludwig, Polman, Chris H., Oksenberg, Jorge R.
フォーマット: Artigo
言語:Inglês
出版事項: Oxford University Press 2009
主題:
Association Studies Articles
オンライン･アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4334814/
https://ncbi.nlm.nih.gov/pubmed/19010793
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn388
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