S55. ANXA11 mutations prevail in Chinese ALS patients with and without cognitive dementia

Amyotrophic lateral sclerosis (ALS) is a fatal neurological disease characterized by progressive paralysis and ultimately respiratory failure within 5 years of symptom onset. Approximately 5–10% of ALS cases exhibit familial inheritance (FALS) and causative gene mutations can be found in 60% of FALS...

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Bibliographic Details
Published in:Clinical neurophysiology, 129.2018, e162-
Main Author: Zhang, Kang (Author)
Other Involved Persons: Liu, Qing ; Liu, Keqiang ; Shen, Dongchao ; Tai, Hongfei ; Shu, Shi ; Ding, Qingyun ; Fu, Hanhui ; Liu, Shuangwu ; Wang, Zhili ; Li, Xiaoguang ; Liu, Mingsheng ; Zhang, Xue ; Cui, Liying ; Guan, Yuzhou
Format: electronic Article
Language:English
ISSN:1872-8952
Physical Description:Online-Ressource
DOI:10.1016/j.clinph.2018.04.415
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