Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: Muscle Weakness and IGHMBP2[original query] |
---|
Variations of IGHMBP2 gene was not the major cause of Han Chinese patients with non-5q-spinal muscular atrophies. Journal of child neurology 2014 Aug 29 (8): NP35-9. Lin Xiang, Zhang Qi-Jie, He Jin, Lin Min-Ting, Murong Shen-Xing, Wang Ning, Chen Wan-J |
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 |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 29, 2024
- Content source: