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McCauley, Joan, Zuvich, J., Beecham, A. H., De Jager, P. L., Konidari, I., Whitehead, P. L., Aubin, C., Ban, M., Pobywajlo, S., Briskin, R., Romano, S., Aggarwal, N., Piccio, L., McArdle, W. L., Strachan, D. P., Evans, D., Cross, A. H., Cree, B., Rioux, J. D., Barcellos, L. F., Ivinson, A. J., Compston, A., Hafler, D. A., Hauser, S. L., Oksenberg, J. R., Sawcer, S. J., Pericak-Vance, M. A. and Haines, J. L. 2010. Comprehensive follow-up of the first genome-wide association study of multiple sclerosis identifies KIF21B and TMEM39A as susceptibility loci. Human Molecular Genetics 19 (5) , pp. 953-962. 10.1093/hmg/ddp542

Bronson, P. G., Caillier, S., Ramsay, P. P., McCauley, Joan, Zuvich, R. L., De Jager, P. L., Rioux, J. D., Ivinson, A. J., Compston, A., Hafler, D. A., Sawcer, S. J., Pericak-Vance, M. A., Haines, J. L., Hauser, S. L., Oksenberg, J. R. and Barcellos, L. F. 2010. CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis. Human Molecular Genetics 19 (11) , pp. 2331-2340. 10.1093/hmg/ddq101

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