Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Mutational spectrum of the CYP1B1 gene in Iranain primary congenital glaucoma family.

Canadian journal of ophthalmology. Journal canadien d'ophtalmologie - 1 Jun 2018

Talebi Farah, Mardasi Farideh Ghanbari, Asl Javad Mohammadi, Lashgari Ali

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Cytochrome P-450 CYP1B1
Share to DNA
Share to DNA Mutational Analysis
Share to Glaucoma

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Intraocular Pressure

Share to Pedigree

Share to Young Adult

Source

Identifiers

PMID: 29784182
DOI: 10.1016/j.jcjo.2017.08.019

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Mutational spectrum of the CYP1B1 gene in Iranain primary congenital glaucoma family.PMID 29784182Read ↗

CYP1B1 mutation profile of Iranian primary congenital glaucoma patients and associated haplotypes.Semantic proximity Read ↗

Meta-analysis of CYP1B1 gene mutations in primary congenital glaucoma patients.Semantic proximity Read ↗

Mutational analysis of CYP1B1 gene in Iranian pedigrees with glaucoma reveals known and novel mutations.Semantic proximity Read ↗

Mutation spectrum of CYP1B1 in Chinese patients with primary open-angle glaucoma.Semantic proximity Read ↗

CYP1B1 gene analysis in primary congenital glaucoma in Indonesian and European patients.Semantic proximity Read ↗

Mutation spectrum of CYP1B1 in North Indian congenital glaucoma patients.Semantic proximity Read ↗

Overview of Cytochrome P450 1B1 gene mutations in patients with primary congenital glaucoma.Semantic proximity Read ↗

Analysis of CYP1B1 Gene Mutations in Patients with Primary Congenital GlaucomaSemantic proximity Read ↗

Mutational spectrum of the CYP1B1 gene in Pakistani patients with primary congenital glaucoma: novel variants and genotype-phenotype correlations.Semantic proximity Read ↗

Mutations in CYP1B1, the Gene for Cytochrome P4501B1, Are the Predominant Cause of Primary Congenital Glaucoma in Saudi ArabiaSemantic proximity Read ↗

Clinical variability of CYP1B1 gene variants in Pakistani primary congenital glaucoma families.Semantic proximity Read ↗

Phenotype and Genotype Correlation in Iranian Primary Congenital Glaucoma Patients.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.