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

Lamination of the Outer Plexiform Layer in Optic Atrophy Caused by Dominant WFS1 Mutations.

Ophthalmology - 1 Jul 2016

Majander Anna, Bitner-Glindzicz Maria, Chan Choi M, Duncan Holly J, Chinnery Patrick F, Subash Malavika, Keane Pearse A, Webster Andrew R, Moore Anthony T, Michaelides Michel, Yu-Wai-Man Patrick

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 DNA
Share to DNA Mutational Analysis
Share to Membrane Proteins
Share to Mutation

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Phenotype

Share to Retinal Ganglion Cells

Share to Tomography, Optical Coherence

Share to Wolfram Syndrome

Source

Open in PubMed Open full text

Identifiers

PMID: 26875006
DOI: 10.1016/j.ophtha.2016.01.007
PMCID: PMC6558247

Genes

WFS1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Lamination of the Outer Plexiform Layer in Optic Atrophy Caused by Dominant WFS1 Mutations.PMID 26875006Read ↗

Peculiar Outer Plexiform Layer in Autosomal Dominant Wolfram Syndrome.Semantic proximity Read ↗

WFS1 in Optic Neuropathies: Mutation Findings in Nonsyndromic Optic Atrophy and Assessment of Clinical Severity.Semantic proximity Read ↗

The phenotypic spectrum of syndromic optic atrophy associated with variants in WFS1: with reclassification of p.Val606Gly as a likely benign variant.Semantic proximity Read ↗

WFS1-Associated Optic Neuropathy: Genotype-Phenotype Correlations and Disease ProgressionSemantic proximity Read ↗

Characteristics of autosomal dominant WFS1-associated optic neuropathy and its comparability to OPA1-associated autosomal dominant optic atrophy.Semantic proximity Read ↗

Thickness mapping of individual retinal layers and sectors by Spectralis SD-OCT in Autosomal Dominant Optic Atrophy.Semantic proximity Read ↗

Autosomal dominant optic neuropathy and sensorineual hearing loss associated with a novel mutation of WFS1.Semantic proximity Read ↗

Fixel-Based Analysis reveals microstructural visual pathway changes associated with retinal remodeling in retinitis pigmentosaSemantic proximity Read ↗

Guidance-cue control of horizontal cell morphology, lamination, and synapse formation in the mammalian outer retina.Semantic proximity Read ↗

Dominant optic atrophy, neuropathy, ataxia, white matter FLAIR hypersignals, middle cerebellar peduncule atrophy and asthenia in OPA1 mutation.Semantic proximity Read ↗

Pattern of retinal ganglion cell loss in dominant optic atrophy due to OPA1 mutations.Semantic proximity Read ↗

Disease boundaries in the retina of patients with Usher syndrome caused by MYO7A gene mutations.Semantic proximity Read ↗

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