Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Sclerosis and POLG[original query] |
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The POLG Polyglutamine Tract Variants in Iranian Patients with Multiple Sclerosis. Iranian journal of child neurology 2015 9 (1): 37-41. Khatami Mehri, Heidari Mohammad Mehdi, Mansouri Reza, Mousavi Fatem |
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 |
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- Page last updated:Apr 22, 2024
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