SATB2 and Global developmental delay: 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.