Tehran University of Medical Sciences

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Faculty Members have conducted research related to the Deep Geno- and Phenotyping in Two Consanguineous Families With Cmt2 Reveals Hadha As an Unusual Disease-Causing Gene and an Intronic Variant in Gdap1 As an Unusual Mutation
Asghar Ghorbani
Asghar Ghorbani

Assistant Professor of Pediatrics

Department Pediatrics

School of Medicine

Baharlou Hospital

Tehran University of Medical Sciences