P.Gly61Glu and P.Arg368His mutations in CYP1B1 that cause congenital glaucoma may be relatively frequent in certain regions of Gilan province, Iran

Purpose: To perform a population-based screening of four CYP1B1 mutations—p.Gly61Glu, p.Arg368His, p.Arg390His, and p.Arg469Trp—in the province of Gilan, Iran. Previous studies have shown that CYP1B1 is a cause of disease in approximately 70% of Iranian patients with primary congenital glaucoma (PCG...

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Bibliographic Details
Main Authors: Mansoure Qashqai, Fatemeh Suri, Mehdi Yaseri, Elahe Elahi
Format: Article
Published: Knowledge E 2018-01-01
Series:Journal of Ophthalmic & Vision Research
Online Access:http://www.jovr.org/article.asp?issn=2008-322X;year=2018;volume=13;issue=4;spage=403;epage=410;aulast=Qashqai