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Article

Mutation spectrum of CYP1B1 in North Indian congenital glaucoma patients.

Molecular vision - 13 Jun 2009

Tanwar Mukesh, Dada Tanuj, Sihota Ramanjit, Das Taposh K, Yadav Usha, Dada Rima

Abstract excerpt

PURPOSE: Mutations in Cytochrome P450 (CYP1B1) are a predominant cause of congenital glaucoma. This study was planned with the aim to identify the mutation profile of CYP1B1 in North Indian primary congenital glaucoma (PCG) patients. METHODS: After ethical clearance, 50 congenital glaucoma patients and 50 ethnically matched controls were recruited in this study. Genomic DNA was isolated from the blood and...

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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

Share to Glaucoma

Share to Polymorphism, Restriction Fragment Length

Share to Sequence Alignment

Share to Sequence Analysis, DNA

Source

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Identifiers

PMID: 19536304
PMCID: PMC2697458

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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