Tehran University of Medical Sciences

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Faculty Members have conducted research related to the A Novel Mutation in the Oxct1 Gene Causing Succinyl-Coa:3-Ketoacid Coa Transferase (Scot) Deficiency Starting With Neurologic Manifestations
Leila Tahernia

Assistant Professor of Pediatrics

Department Pediatrics

School of Medicine

Childrens Medical Center

Tehran University of Medical Sciences

All Documents
8. The First Febrile Seizure; Predisposing Factors and Recurrence Rate, Iranian Journal of Child Neurology (2021)