Tehran University of Medical Sciences

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Faculty Members have conducted research related to the Crystallographic Modeling of the Pnpt1:C.1453A>G Variant As a Cause of Mitochondrial Dysfunction and Autosomal Recessive Deafness; Expanding the Neuroimaging and Clinical Features
Alireza Biglari
Alireza Biglari

Professor of Genetics

Department Medical Genetics

School of Medicine

Tehran University of Medical Sciences

All Documents
17. Kh Domain Containing 3 Like (Khdc3l) Frame-Shift Mutation Causes Both Recurrent Pregnancy Loss and Hydatidiform Mole, European Journal of Obstetrics and Gynecology and Reproductive Biology (2021)