HuGE Literature Finder
Records
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Mutations in UBQLN2 and SIGMAR1 genes are rare in Korean patients with amyotrophic lateral sclerosis. Neurobiology of aging 2014 Aug 35 (8): 1957.e7-8. Kim Hee-Jung, Kwon Min-Jung, Choi Won-Jun, Oh Ki-Wook, Oh Seong-Il, Ki Chang-Seok, Kim Seung Hy |
Association of UBQLN1 mutation with Brown-Vialetto-Van Laere syndrome but not typical ALS. Neurobiology of disease 2012 Dec 48 (3): 391-8. González-Pérez Paloma, Lu Yubing, Chian Ru-Ju, Sapp Peter C, Tanzi Rudolph E, Bertram Lars, McKenna-Yasek Diane, Gao Fen-Biao, Brown Robert |
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- Page last updated:Feb 07, 2023
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