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Faculty Members have conducted research related to the Identification of a Novel Stop Loss Mutation in P2rx2 Gene in an Iranian Family With Autosomal Nonsyndromic Hearing Loss

Zahra Rezai

Professor of Infertility & IVF

Department Obstetrics and Gynecology

School of Medicine

Yas Hospital

Tehran University of Medical Sciences

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1. Novel Co-Occurrence of Slc26a4 and Kctd7 Variants in a Pediatric Patient With Syndromic Hearing Loss and Myoclonic Epilepsy, Egyptian Journal of Medical Human Genetics (2025)

2. Neonatal Seizure: How Reliable Is Its Diagnosis and Treatment? a Mini Review of Previous Knowledge, Iranian Journal of Child Neurology (2020)

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Zahra Rezai

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