Biblio
ALS-causative mutations in FUS/TLS confer gain and loss of function by altered association with SMN and U1-snRNP. Nat Commun. 2015;6:6171.
The APP intracellular domain promotes expression to enable feed-forward neurodegenerative mechanisms in Parkinson's disease. Sci Signal. 2022;15(748):eabk3411.