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. 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: 18 may. 2024.