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Article

Screening of common CYP1B1 mutations in Iranian POAG patients using a microarray-based PrASE protocol.

Molecular vision - 1 Jan 2008

Suri Fatemeh, Kalhor Reza, Zargar Seyed Jalal, Nilforooshan Navid, Yazdani Shahin, Nezari Hossein, Paylakhi Seyed Hassan, Narooie-Nejhad Mehrnaz, Bayat Behnaz, Sedaghati Tina, Ahmadian Afshin, Elahi Elahe

Abstract excerpt

PURPOSE: The gene coding cytochrome P4501B1 (CYP1B1) has been shown to be a major cause of primary congenital glaucoma in the Iranian population. More recently it was shown to also be important in juvenile-onset open angle glaucoma (JOAG). We aimed to further investigate the role of CYP1B1 in a larger cohort of primary open angle glaucoma (POAG) patients which included late-onset patients. We also aimed to set up...

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Share to Aryl Hydrocarbon Hydroxylases
Share to Cytochrome P-450 CYP1B1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cytochrome P-450 Enzyme System

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Source

Open in PubMed Open full text

Identifiers

PMID: 19096718
PMCID: PMC2603445

Genes

MYOC

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

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