Determination of the real effect of genes identified in GWAS: The example of IL2RA in multiple sclerosis by Babron, M, Babron, M, Perdry, H, Perdry, H, Handel, A, Ramagopalan, S, Damotte, V, Damotte, V, Damotte, V, Fontaine, B, Fontaine, B, Fontaine, B, Müller-Myhsok, B, Ebers, G, Clerget-Darpoux, F, Clerget-Darpoux, F

Determination of the real effect of genes identified in GWAS: the example of IL2RA in multiple sclerosis. by Babron, M, Perdry, H, Handel, A, Ramagopalan, S, Damotte, V, Fontaine, B, Müller-Myhsok, B, Ebers, G, Clerget-Darpoux, F

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis. by Sawcer, S, Hellenthal, G, Pirinen, M, Spencer, C, Patsopoulos, N, Moutsianas, L, Dilthey, A, Su, Z, Freeman, C, Hunt, SE, Edkins, S, Gray, E, Booth, DR, Potter, S, Goris, A, Band, G, Oturai, AB, Strange, A, Saarela, J, Bellenguez, C, Fontaine, B, Gillman, M, Hemmer, B, Gwilliam, R, Zipp, F

Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis. by Beecham, A, Patsopoulos, N, Xifara, D, Davis, M, Kemppinen, A, Cotsapas, C, Shah, T, Spencer, C, Booth, D, Goris, A, Oturai, A, Saarela, J, Fontaine, B, Hemmer, B, Martin, C, Zipp, F, D'Alfonso, S, Martinelli-Boneschi, F, Taylor, B, Harbo, H, Kockum, I, Hillert, J, Olsson, T, Ban, M, Oksenberg, JR

Impaired presynaptic high-affinity choline transporter causes a congenital myasthenic syndrome with episodic apnea by Bauché, S, O'Regan, S, Azuma, Y, Laffargue, F, McMacken, G, Sternberg, D, Brochier, G, Buon, C, Bouzidi, N, Topf, A, Lacène, E, Remerand, G, Beaufrere, A-M, Pebrel-Richard, C, Thevenon, J, El Chehadeh-Djebbar, S, Faivre, L, Duffourd, Y, Ricci, F, Mongini, T, Fiorillo, C, Astrea, G, Burloiu, CM, Butoianu, N, Sandu, C, Servais, L, Bonne, G, Nelson, I, Desguerre, I, Nougues, M-C, Bœuf, B, Romero, N, Laporte, J, Boland, A, Lechner, D, Deleuze, J-F, Fontaine, B, Strochlic, L, Lochmuller, H, Eymard, B, Mayer, M, Nicole, S