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

Prevalence of optineurin sequence variants in adult primary open angle glaucoma: implications for diagnostic testing.

Journal of medical genetics - 1 Aug 2003

Aung T, Ebenezer N D, Brice G, Child A H, Prescott Q, Lehmann O J, Hitchings R A, Bhattacharya S S

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 Eye Proteins
Share to Genetic Heterogeneity
Share to Glaucoma
Share to Glaucoma, Open-Angle

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Intraocular Pressure

Share to Protein Isoforms

Share to Transcription Factor TFIIIA

Share to United Kingdom

Source

Open in PubMed Open full text

Identifiers

PMID: 12920093
DOI: 10.1136/jmg.40.8.e101
PMCID: PMC1735547

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

Prevalence of optineurin sequence variants in adult primary open angle glaucoma: implications for diagnostic testing.PMID 12920093Read ↗

Evaluation of optineurin sequence variations in 1,048 patients with open-angle glaucomaSemantic proximity Read ↗

Optineurin coding variants in Ghanaian patients with primary open-angle glaucoma.Semantic proximity Read ↗

Update on the genetics of primary open-angle glaucomaSemantic proximity Read ↗

Analysis of rare variants and common haplotypes in the optineurin gene in Swedish glaucoma cases.Semantic proximity Read ↗

Adult-onset primary open-angle glaucoma caused by mutations in optineurin.Semantic proximity Read ↗

Defining the pathogenicity of optineurin in juvenile open-angle glaucoma.Semantic proximity Read ↗

Distribution of optineurin sequence variations in an ethnically diverse population of low-tension glaucoma patients from the United States.Semantic proximity Read ↗

Clinical implications of recent advances in primary open-angle glaucoma geneticsSemantic proximity Read ↗

Lack of association between optineurin gene variants T34T, E50K, M98K, 691_692insAG and R545Q and primary open angle glaucoma in Brazilian patients.Semantic proximity Read ↗

Analysis of optineurin (OPTN) gene mutations in subjects with and without glaucoma: the Blue Mountains Eye Study.Semantic proximity Read ↗

Variation in optineurin (OPTN) allele frequencies between and within populations.Semantic proximity Read ↗

Evaluation of Optineurin as a candidate gene in Indian patients with primary open angle glaucoma.Semantic proximity Read ↗

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