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...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Τόπος έκδοσης:Hum Mol Genet
Κύριοι συγγραφείς: 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.
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: Oxford University Press 2009
Θέματα:
Association Studies Articles
Διαθέσιμο Online: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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