Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: TRIM2[original query] |
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ALS5/SPG11/KIAA1840 mutations cause autosomal recessive axonal Charcot-Marie-Tooth disease. Brain : a journal of neurology 2015 Nov . Montecchiani Celeste, Pedace Lucia, Lo Giudice Temistocle, Casella Antonella, Mearini Marzia, Gaudiello Fabrizio, Pedroso José L, Terracciano Chiara, Caltagirone Carlo, Massa Roberto, St George-Hyslop Peter H, Barsottini Orlando G P, Kawarai Toshitaka, Orlacchio Anton |
Genome-wide meta-analysis reveals novel susceptibility loci for thyrotoxic periodic paralysis.
European journal of endocrinology 2020 Dec 183 (6): 607-617. Hoi-Yee Li Gloria, Cheung Ching-Lung, Zhao Shuang-Xia, Song Huai-Dong, Wai-Chee Kung Ann |
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