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As such, FOXG1 is implicated in an extensive spectral range of congenital brain disorders, like the congenital variant of Rett syndrome, infantile spasms, microcephaly, autism spectrum disorder (ASD) and schizophrenia. Recent technical improvements have actually yielded higher insight into phenotypic variations observed in FOXG1 syndrome, molecular components fundamental pathogenesis for the illness, and multifaceted roles of FOXG1 phrase. In this review, we explore the p
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