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Autor:
Pooneh Nikuei, Ph.D., Zahra Khashavy, Mohammad Ali Farazi Fard, Shahrzad Tabasi4 Pharm.D. Student, Ari Zeidi5 B.Sc. Student, Parnian Pourkashani, Zahra Tabatabaei, Ebrahim Eftekhar, Mozhgan Saberi, Frouzandeh Mahjoubi
Publikováno v:
International Journal of Reproductive BioMedicine, Vol 21, Iss 8, Pp 667-672 (2023)
Abstract Background: Sex determining region Y box transcription factor 2 (SOX2) mutations lead to bilateral anophthalmia with autosomal dominant human inheritance. SOX2 mutations could result in severe ocular phenotypes usually associated with variab
Externí odkaz:
https://doaj.org/article/7477202e018c48f4a7ae1e39de3a5b01