Fig. 1From: Rare TBK1 variants in patients with frontotemporal dementia and amyotrophic lateral sclerosis in a Chinese cohortSanger sequencing showed two nover TBK1 novel mutations. a mutation c.1959_1960insGT, p.E653fs in a sporadic case with FTD-ALS; b mutation c.2063_2064delTT, p.L688Rfs*14 in an ALS-FTD familyBack to article page