Cystatin B (CSTB) is a ubiquitous protein belonging to a superfamily of protease inhibitors. CSTB may play a critical role in brain physiology because its mutations cause progressive myoclonic epileps
A recurrent de novo mutation in the transcriptional corepressor CTBP1 is associated with neurodevelopmental disabilities in children (Beck et al., 2016; Beck et al., 2019; Sommerville et al., 2017).
Gene-editing technologies have made it feasible to create nonhuman primate models for human genetic disorders. Here we report detailed genotypes and phenotypes of TALEN-edited MECP2 mutant cynomolgus