| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6022440 | Neurobiology of Disease | 2012 | 8 Pages |
Abstract
⺠Genetic variants in UBQLN1 are not associated with amyotrophic lateral sclerosis. ⺠Novel UBQLN1 mutation (E54D) in a patient with atypical motor neuron disease. ⺠Dysfunction in the UPS may contribute to the pathogenesis of BVVLS.
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Neurology
Authors
Paloma González-Pérez, Yubing Lu, Ru-Ju Chian, Peter C. Sapp, Rudolph E. Tanzi, Lars Bertram, Diane McKenna-Yasek, Fen-Biao Gao, Robert H. Jr.,