Paper Details

Science Communicator Platform

Stay connected! Follow us on X network (Twitter):

Faculty Members have conducted research related to the A Case of a 6-Year-Old Girl With a Rare Compound Heterozygous Mutation of Kctd7 Presenting With Progressive Myoclonic Epilepsy

Zahra Rezai

Professor of Infertility & IVF

Department Obstetrics and Gynecology

School of Medicine

Yas Hospital

Tehran University of Medical Sciences

All Documents

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)

Science Communicator Platform

Zahra Rezai

Related Documents

All Documents