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

Conclusion The current study further endorses the role of CYP1B1 mutations in the etiology of PCG among Egyptian patients and is the first study to report MYOC gene mutation in Egyptian patients with PCG.

Source: Egyptian Journal of Medical Human Genetics - August 27, 2016 Category: Genetics & Stem Cells Source Type: research