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Publication date
2016 Oct 19
Authors
Antel, J Ban, M Baranzini, S Barcellos, L Barizzone, N Beecham, A Berge, T Bernardinelli, L Booth, D Bos, S Buck, D Butkiewicz, M Celius, EG Comabella, M Compston, A Dedham, K Cotsapas, C Alfonso, SD De Jager, P Dubois, B Duquette, P Fontaine, B Gasperi, C Gil, E Goris, A Gourraud, PA Graetz, C Gyllenberg, A Hadjigeorgiou, G Hafler, D Hribko, D Haines, J Harbo, H Hauser, S Warto, S Hawkins, C Hemmer, B Henry, R Hintzen, R Horakova, D Ivinson, A Howard, M Jelcic, I Kaskow, B Kira, JI Kleinova, P Kockum, I Kucerova, K Lill, C Luessi, F Malhotra, S Martin, R Martinelli, F Matsushita, T McCabe, C McCauley, J Mescheriakkova, J Mitrovic, M Moen, SM Montalban, X Muhlau, M Nakmura, Y Oksenberg, J Olsson, T Oturai, A Palotie, A Patsopoulos, N Pavlicova, J Pericak-Vance, P Piehl, F Rebeix, I Rioux, J Saarela, J Sawcer, S Sellebjerg, F Sondergaard, HB Sorensen, PS Sospedra, M Spurkland, A Stewart, G Taylor, B Uitterlinden, A Van Duijn, C Zipp, F
Group authors
Int Multiple Sclerosis Genetics Co
Author KI Usernames
Gyllenberg, A|altamm Kockum, I|ingkoc Olsson, T|tomols Piehl, F|frepie
Pubmed ID
27764667
Journal
Neuron
Doctype
Article
KI Connection
Låg
Mesh SV
Multipel skleros Mutation Människa Polymorfism, enkelnukleotid Risk
Mesh EN
Multiple Sclerosis Mutation Polymorphism, Single Nucleotide Risk
First date
2016-11-20T10:47:17.783Z