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