As deletion in the transcription factor Satb2 leads to the development of epilepsy and developmental delay in people [19,49] and duplication of Satb2 can also induce epilepsy and autistic behavior [50], the importance of investigation of the molecular and cellular mechanisms of the Satb2 effect in the brain leading to the induction of neurodegenerative processes is apparent. Here, SATB2 is linked to epilepsy.