Myocilin Mutations Are Not a Major Cause of Primary Congenital Glaucoma in Iranian Patients

Myocilin Mutations Are Not a Major Cause of Primary Congenital Glaucoma in Iranian Patients

Purpose: To assess the frequency of mutations in the Myocilin (MYOC) gene in Iranian patients affected with primary congenital glaucoma (PCG). Methods: The individuals evaluated herein are among a larger cohort of 100 patients who had previously been screened for CYP1B1 mutations. Eighty subjects c...

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Bibliographic Details
Main Authors: Elahe Elahi, Mehrnaz Narooie-Nejhad, Fatemeh Suri, Shahin Yazdani
Format: Article
Language:English
Published: Knowledge E 2010-01-01
Series:Journal of Ophthalmic & Vision Research
Subjects:
Primary Congenital Glaucoma; Myocilin
Online Access:http://www.jovr.org/article.asp?issn=2008-322X;year=2010;volume=5;issue=2;spage=101;epage=104;aulast=Elahi

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