A complete genomic screen for multiple sclerosis underscores a role for the major histocompatability complex

Author:

Haines J.L.,Ter-Minassian M.,Bazyk A.,Gusella J.F.,Kim D.J.,Terwedow H.,PericakVance M.A.,Rimmler J.B.,Haynes C.S.,Roses A.D.,Lee A.,Shaner B.,Menold M.,Seboun E.,Fitoussi R-P.,Gartioux C.,Reyes C.,Ribierre F.,Gyapay G.,Weissenbach J.,Hauser S.L.,Goodkin D.E.,Lincoln R.,Usuku K.,Garcia-Merino A.,Gatto N.,Young S.,Oksenberg J.R.

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Reference33 articles.

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2. Hauser, S.L. et al. Analysis of human T lymphotropic virus sequences in multiple sclerosis. Nature 322, 176–177 (1986).

3. Ebers, G.C. & Sadovnick, A.D. The role of genetic factors in multiple sclerosis susceptibility. J.Neuroimmunol. 54, 1017 (1994).

4. Ebers, G.C., Sadovnick, A.D. & Risch, N.J. A genetic basis for familial aggregation in multiple sclerosis. Nature 377, 150–151 (1995).

5. Risch, N. Linkage strategies for genetically complex traits. III. The effect of marker polymorphism on analysis of affected relative pairs. Am. J. Hum. Genet. 46, 242–253 (1990).

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