Nader Mansour Samaei
3PUBLICATIONS
4CO-AUTHORS
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Publications (3)
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|Nov 29, 2024
A novel frameshift variant in the TMPRSS3 gene causes nonsyndromic hearing loss in a consanguineous family.Nahid Rezaie, Saeedeh Sadat Ghazanfari, Seyede Mahsa Mousavikia
|May 20, 2024
Identification of novel and known genetic variants associated with hereditary hearing loss in iranian families using whole exome sequencing.Nahid Rezaie, Nader Mansour Samaei, Morteza Oladnabi
|Nov 14, 2021
A case report of Ring chromosome 18 with systemic Lupus Erythematosus and Crohn's disease.Tina Rezaeizadeh, Encieh Delshad, Nader Mansour Samaei
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