Tehran University of Medical Sciences

Science Communicator Platform

Faculty Members have conducted research related to the Novel Mutation of Slc37a4 in a Glycogen Storage Disease Type Ib Patient With Neutropenia, Horseshoe Kidney, and Arteriovenous Malformation: A Case Report
Fatemeh Tahghighi
Fatemeh Tahghighi

Associate Professor of Pediatrics Rheumatology

Department Pediatrics

School of Medicine

Childrens Medical Center

Tehran University of Medical Sciences

Related Documents
1. Post-Mortem Diagnosis of Heme Oxygenase-1 Deficiency by Whole Exome Sequencing in an Iranian Child, International Journal of Molecular and Cellular Medicine (2019)
All Documents
12. A Boy With Limping and Hip Pain, Iranian Journal of Pediatrics (2021)
16. Post-Mortem Diagnosis of Heme Oxygenase-1 Deficiency by Whole Exome Sequencing in an Iranian Child, International Journal of Molecular and Cellular Medicine (2019)