Discover Community Create You

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

Bietti Crystalline Retinopathy Confirmed by Mutation of CYP4V2 Gene in a Korean Patient.

Korean journal of ophthalmology : KJO - 1 Feb 2016

Park Young Joo, Hwang Duck Jin, Seong Moon-Woo, Park Sung Sup, Woo Se Joon

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 Corneal Dystrophies, Hereditary
Share to Cytochrome P450 Family 4
Share to Fluorescein Angiography
Share to Republic of Korea

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Retinal Diseases

Share to Retinal Pigment Epithelium

Share to Tomography, Optical Coherence

Share to Visual Acuity

Source

Open in PubMed Open full text

Identifiers

PMID: 26865810
DOI: 10.3341/kjo.2016.30.1.81
PMCID: PMC4742652

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Bietti Crystalline Retinopathy Confirmed by Mutation of CYP4V2 Gene in a Korean Patient.PMID 26865810Read ↗

Clinical and molecular findings in three Japanese patients with crystalline retinopathy.Semantic proximity Read ↗

Clinical and genetic characterization of a large cohort of Chinese patients with Bietti crystalline retinopathy.Semantic proximity Read ↗

PREDICTED PROTEIN STRUCTURE VARIATIONS INDICATE THE CLINICAL PRESENTATION OF CYP4V2-RELATED BIETTI CRYSTALLINE DYSTROPHY.Semantic proximity Read ↗

A novel mutation in the CYP4V2 gene in a Chinese patient with Bietti's crystalline dystrophy.Semantic proximity Read ↗

Expanding the Phenotypic and Genotypic Spectrum of Bietti Crystalline Dystrophy.Semantic proximity Read ↗

Bietti crystalline corneoretinal dystrophy associated with CYP4V2 gene mutations.Semantic proximity Read ↗

Identification of CYP4V2 mutation in 36 Chinese families with Bietti crystalline corneoretinal dystrophy.Semantic proximity Read ↗

Unravelling CYP4V2: Clinical features, genetic insights, pathogenic mechanisms and therapeutic strategies in Bietti crystalline corneoretinal dystrophySemantic proximity Read ↗

Genetics of Bietti Crystalline Dystrophy.Semantic proximity Read ↗

Bietti crystalline corneoretinal dystrophy is caused by mutations in the novel gene CYP4V2.Semantic proximity Read ↗

Identification of novel CYP4V2 genotypes associated with Bietti crystalline dystrophy and atypical anterior segment phenotypes in Spanish patients.Semantic proximity Read ↗

Identification of CYP4V2 mutation in 21 families and overview of mutation spectrum in Bietti crystalline corneoretinal dystrophy.Semantic proximity Read ↗

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