CYP1B1 and myocilin gene mutations in Egyptian patients with primary congenital glaucoma

Mahmoud R. Fassad; Asmaa K. Amin; Heba A. Morsy; Noha M. Issa; Nader H. Bayoumi; Sahar A. El Shafei; Soha F. Kholeif

doi:10.1016/j.ejmhg.2016.07.003

10.1016/j.ejmhg.2016.07.003 383 المشاهدات 6 الاقتباسات

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الاستشهاد بهذا المقال (APA)

Mahmoud, R. F., Asmaa, K. A., Heba, A. M., Noha, M. I., Nader, H. B., Sahar, A. E. S., Soha, F. K. (2017). CYP1B1 and myocilin gene mutations in Egyptian patients with primary congenital glaucoma. Egyptian Journal of Medical Human Genetics. https://doi.org/10.1016/j.ejmhg.2016.07.003

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