Human Genome Epidemiology Literature Finder
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Query Trace: Motor Neuron Disease and SIGMAR1[original query] |
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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 |
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- Page last updated:Jun 02, 2023
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