Tehran University of Medical Sciences

Science Communicator Platform

Faculty Members have conducted research related to the A Novel Homozygous Variant in the Polr1a Gene: A Complicated Hereditary Spastic Paraplegia (C-Hsp) or a Hypomyelinating Leukodystrophy Type-27 (Hld27) Phenotype?
Sara Ranji
Sara Ranji

Assistant Professor of Neurology

Department Neurology

School of Medicine

Imam Khomeini Hospital Complex

Iranian Center of Neurological Research

Tehran University of Medical Sciences

All Documents
14. Novel Abcd1 Gene Mutations in Iranian Pedigrees With X-Linked Adrenoleukodystrophy, Journal of Pediatric Endocrinology and Metabolism (2019)
16. Experimental Detection of Muscle Atrophy Initiation Using Semg Signals, Middle East Conference on Biomedical Engineering# MECBME (2018)