摘要
Amyotrophic lateral sclerosis (ALS) is a devastating neurodegenerative disease characterized by the progressive loss of both upper and lower motor neurons.Most ALS cases are sporadic,but approximately 5-10%of patients have a familial background.To date,more than 30 familial ALS-causative genes have been identified (Maurel et al., 2018).
基金
the JSPS KAKENHI,grant numbers20H03593 (to KK) and 21H02706 (to MK)
Takeda Science Foundation (to KK)。