AMIRKASHANI, Davoud; ASADOLLAHI, Mostafa; HOSSEINI, Rozita; TALEBI, Saeed; GOLCHEHRE, Zahra; KERAMATIPOUR, Mohammad. A Novel Mutation in the OXCT1 Gene Causing Succinyl-CoA:3-Ketoacid CoA Transferase (SCOT) Deficiency Starting with Neurologic Manifestations. Iranian Journal of Child Neurology, [S. l.], v. 17, n. 2, p. 127–133, 2023. DOI: 10.22037/ijcn.v17i2.35963. Disponível em: https://journals.sbmu.ac.ir/ijcn/article/view/35963. Acesso em: 8 jul. 2026.