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

OPA1 Dominant Optic Atrophy: Pathogenesis and Therapeutic Targets.

Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society - 1 Dec 2023

Wong David C S, Harvey Joshua P, Jurkute Neringa, Thomasy Sara M, Moosajee Mariya, Yu-Wai-Man Patrick, Gilhooley Michael J

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 GTP Phosphohydrolases
Share to Mutation
Share to Optic Atrophy
Share to Optic Atrophy, Autosomal Dominant

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Source

Open in PubMed Open full text

Identifiers

PMID: 37974363
DOI: 10.1097/WNO.0000000000001830
PMCID: PMC10645107

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 25 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

OPA1 Dominant Optic Atrophy: Pathogenesis and Therapeutic Targets.PMID 37974363Read ↗

Dominant optic atrophy: novel OPA1 mutations and revised prevalence estimates.Semantic proximity Read ↗

Dominant optic atrophy: updates on the pathophysiology and clinical manifestations of the optic atrophy 1 mutation.Semantic proximity Read ↗

Targeting the OPA1 pathway in Autosomal Dominant Optic Atrophy (ADOA): 25 years from gene discovery to therapeutic strategy.Semantic proximity Read ↗

Multiple sclerosis-like disorder in OPA1-related autosomal dominant optic atrophy.Semantic proximity Read ↗

Dominant optic atrophySemantic proximity Read ↗

OPA1: How much do we know to approach therapy?Semantic proximity Read ↗

A phenotypic variation of dominant optic atrophy and deafness (ADOAD) due to a novel OPA1 mutation.Semantic proximity Read ↗

Heterozygous type 1 Autosomal Dominant Optic Atrophy (ADOA) with OPA1 c.1936-2A>G genetic variant.Semantic proximity Read ↗

Deletion of the OPA1 gene in a dominant optic atrophy family: evidence that haploinsufficiency is the cause of disease.Semantic proximity Read ↗

[Not only optic neuropathy: new molecular and clinical aspects of OPA1 gene mutations].Semantic proximity Read ↗

Biallelic Optic Atrophy 1 (OPA1) Related Disorder-Case Report and Literature Review.Semantic proximity Read ↗

The prevalence and natural history of dominant optic atrophy due to OPA1 mutations.Semantic proximity Read ↗

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