Rare TBK1 variants in patients with frontotemporal dementia and amyotrophic lateral sclerosis in a Chinese cohort

ConclusionsThis study enlarges the genetic and phenotypic spectrum ofTBK1 mutation in a Chinese cohort. Our data indicates thatTBK1 mutation is not a common cause for ALS and FTD in Chinese patients.

http://link.springer.com/10.1186/s40035-018-0136-6

Source: Translational Neurodegeneration - December 4, 2018 Category: Neurology Source Type: research