Next-generation sequencing for detection of mutations associated with rare disorders in patients meeting diagnostic criteria for primary progressive multiple sclerosis
Weisfeld-Adams, J.D, Ludtke, A, Scott, S.A, Katzsand, I, Naik, H, Linderman, M.D, Paizan-Ruiz, C, Wasserstein, M.P, Shi, L, Brandt, T, McGraw, C.A, Kornreich, R, Farrell, C, Schadt, E.E, Lublin, F.D, Oksenberg, J.S
Published in Journal of the neurological sciences (15.10.2013)
Published in Journal of the neurological sciences (15.10.2013)
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