Tehran University of Medical Sciences

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):
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
Mohammad Kazem Bakhshandeh-Bali
Mohammad Kazem Bakhshandeh-Bali

Assistant Professor of Pediatric Neurology

Department Pediatrics

School of Medicine

Hakim Children Hospital,Baharlou Hospital

Tehran University of Medical Sciences