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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Detalhes bibliográficos
Publicado no:Hum Mol Genet
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2009
Assuntos:
Association Studies Articles
Acesso em linha: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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