Amirkashani, D.; Asadollahi, M.; Hosseini, R.; Talebi, S.; Golchehre, Z.; Keramatipour, M. A Novel Mutation in the OXCT1 Gene Causing Succinyl-CoA:3-Ketoacid CoA Transferase (SCOT) Deficiency Starting With Neurologic Manifestations. Iran J Child Neurol 2023, 17, 127-133.