NR2F1 and Bosch-Boonstra-Schaaf optic atrophy syndrome: Previous studies showed that NR2F1 point mutation caused neurodevelopmental disorders diseases such as Bosch‐Boonstra‐Schaaf optic atrophy syndrome (BBSOAS) in vivo,31 which suggests that the NR2F1 was vital in the development of the nervous system.