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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Bibliografiska uppgifter
I publikationen:Hum Mol Genet
Huvudupphovsmän: 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.
Materialtyp: Artigo
Språk:Inglês
Publicerad: Oxford University Press 2009
Ämnen:
Association Studies Articles
Länkar: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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