Tehran University of Medical Sciences

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Faculty Members have conducted research related to the Novel Digital Anomalies, Hippocampal Atrophy, and Mutations Expand the Genotypic and Phenotypic Spectra of Cnksr2 in the Houge Type of X-Linked Syndromic Intellectual Development Disorder (Mrxshg)
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

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