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...
|Published in:||Clinical neurophysiology, 129.2018, e162-|
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