Article
TDP-43 pathology and functional deficits in wild-type and ALS/FTD mutant cyclin F mouse models.
Neuropathology and applied neurobiology - 1 Apr 2023
van Hummel Annika, Sabale Miheer, Przybyla Magdalena, van der Hoven Julia, Chan Gabriella, Feiten Astrid F, Chung Roger S, Ittner Lars M, Ke Yazi D
Abstract excerpt
AIMS: Amyotrophic lateral sclerosis (ALS) is characterised by a progressive loss of upper and lower motor neurons leading to muscle weakness and eventually death. Frontotemporal dementia (FTD) presents clinically with significant behavioural decline. Approximately 10% of cases have a known family history, and disease-linked mutations in multiple genes have been identified in FTD and ALS. More recently, ALS and...
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