Cytochrome P450 Family 1 B1 Gene Mutations in Primary Congenital Glaucoma Affected Egyptian Patients
Amanne Feisal Esmael, Hanaa Abdel-Sadek Oraby & Soheir Mohamed El Nahas · Ophthalmology Research: An International Journal · 2019
Aims: Primary congenital glaucoma (PCG) is a leading cause of childhood blindness. The cytochrome P450 family 1, subfamily B, polypeptide 1 (CYP1B1) is the most mutated gene that is associated with PCG. Very few studies have examined the promoter region and exon1 of the CYP1B1 ge...
Open access
Research Article
10.9734/or/2019/v11i130120