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Amirkashani, D., Asadollahi, M., Hosseini, R., Talebi, S., Golchehre, Z. and Keramatipour, M. 2023. 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. 17, 2 (May 2023), 127–133. DOI:https://doi.org/10.22037/ijcn.v17i2.35963.