✦ LIBER ✦
Next-generation sequencing for detection of mutations associated with rare disorders in patients meeting diagnostic criteria for primary progressive multiple sclerosis
✍ Scribed by 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.
- Book ID
- 121987571
- Publisher
- Elsevier Science
- Year
- 2013
- Tongue
- English
- Weight
- 66 KB
- Volume
- 333
- Category
- Article
- ISSN
- 0022-510X
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