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

The central retinal thickness and its related genotype in ABCA4-related retinopathy.

Eye (London, England) - 1 Oct 2024

Wang Yimin, Li Tong, Yu Suqin, Gong Yuanyuan, Zhang Min, Wu Yidong, Liu Wenjia, Sun Junran, Chen Jieqiong, Sun Xiaodong

Abstract excerpt

PURPOSE: To further explore the influence of genotype, including mutation type and structural domain, on the severity of macular atrophy, we measured the central retinal thickness (CRT) in patients with ABCA4-related retinopathy. METHODS: A total of 66 patients were included in the cohort. This was a retrospective investigation. The patients were tested using whole exon sequencing and ophthalmic exams, including...

Read the complete abstract on PubMed

Topics

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

Share to ATP-Binding Cassette Transporters
Share to Child

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to DNA Mutational Analysis

Share to Fluorescein Angiography

Share to Retina

Share to Tomography, Optical Coherence

Share to Visual Acuity

Share to Young Adult

Source

Open in PubMed Open full text

Identifiers

PMID: 38740961
DOI: 10.1038/s41433-024-03104-2
PMCID: PMC11427577

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.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

The central retinal thickness and its related genotype in ABCA4-related retinopathy.PMID 38740961Read ↗

Genetic and Clinical Features of ABCA4-Associated Retinopathy in a Japanese Nationwide Cohort.Semantic proximity Read ↗

Genotypes Predispose Phenotypes-Clinical Features and Genetic Spectrum of ABCA4-Associated Retinal Dystrophies.Semantic proximity Read ↗

Association Between Genotype and Phenotype Severity in ABCA4-Associated Retinopathy.Semantic proximity Read ↗

Genotypic profile and phenotype correlations of ABCA4-associated retinopathy in Koreans.Semantic proximity Read ↗

Clinical spectrum, genetic complexity and therapeutic approaches for retinal disease caused by ABCA4 mutations.Semantic proximity Read ↗

Stargardt disease-associated mutation spectrum of a Russian Federation cohort.Semantic proximity Read ↗

[Inherited retinal diseases in patients with ABCA4 gene mutations].Semantic proximity Read ↗

Characterization of the Subclinical Perilesional Zone in the Macula of Early-Stage ABCA4 DiseaseSemantic proximity Read ↗

Clinical Observation and Genotype-Phenotype Analysis of ABCA4- Related Hereditary Retinal Degeneration before Gene Therapy.Semantic proximity Read ↗

Peripheral pigmented lesions in ABCA4-associated retinopathy.Semantic proximity Read ↗

Clinical and genetic analysis of the ABCA4 gene associated retinal dystrophy in a large Chinese cohort.Semantic proximity Read ↗

Genotypic spectrum of ABCA4-associated retinal degenerations in 211 unrelated Mexican patients: identification of 22 novel disease-causing variants.Semantic proximity Read ↗

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