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NEK1 loss-of-function mutation induces DNA damage accumulation in ALS patient-derived motoneurons
Stem Cell Research
A B S T R A C T Mutations in genes coding for proteins involved in DNA damage response (DDR) and repair, such as C9orf72 and FUS (Fused in Sarcoma), are associated with neurodegenerative diseases and lead to amyotrophic lateral sclerosis (ALS). Heterozygous loss-of-function mutations in NEK1 (NIMA-related kinase 1) have also been recently found to cause ALS. NEK1 codes for a multifunctional protein, crucially involved in mitotic checkpoint control and DDR. To resolve pathological alterationsdoi:10.1016/j.scr.2018.06.005 pmid:29929116 fatcat:zwrexal7e5evxh4udiqngcxt44