Tehran University of Medical Sciences

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Faculty Members have conducted research related to the A Case of a 6-Year-Old Girl With a Rare Compound Heterozygous Mutation of Kctd7 Presenting With Progressive Myoclonic Epilepsy
Mahmood Mohamadi
Mahmood Mohamadi

Professor of Pediatric Neurology

Department Pediatrics

School of Medicine

Childrens Medical Center

Tehran University of Medical Sciences

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