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

Atypical Late-Onset Leber Hereditary Optic Neuropathy (LHON) Associated With T14484C Mutation.

Journal of neuro-ophthalmology : the official journal of the North American Neuro-Ophthalmology Society - 1 Jun 2024

Yasin Anas L, Mendoza-Santiesteban Carlos E, Khodeiry Mohamed M, Lam Byron L

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, Mitochondrial
Share to DNA Mutational Analysis
Share to Mutation
Share to Optic Atrophy, Hereditary, Leber

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Open in PubMed Open full text

Identifiers

PMID: 38741248
DOI: 10.1097/WNO.0000000000001835
PMCID: PMC11081469

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Atypical Late-Onset Leber Hereditary Optic Neuropathy (LHON) Associated With T14484C Mutation.PMID 38741248Read ↗

A Rare Mutation Associated With Probable Late-Onset Leber's Hereditary Optic Neuropathy.Semantic proximity Read ↗

[Research progress of Leber hereditary optic neuropathy].Semantic proximity Read ↗

[Leber hereditary optic neuropathy: update on genetics and pathomechanisms].Semantic proximity Read ↗

Leber hereditary optic neuropathy-new insights and old challenges.Semantic proximity Read ↗

[Clinical practice guidelines for Leber's hereditary optic neuropathy].Semantic proximity Read ↗

Progress in diagnosis and treatment of Leber's hereditary optic neuropathy.Semantic proximity Read ↗

Variable Presentation of Leber Hereditary Optic Neuropathy in Children of a Family Harboring a Rare m.13051G>A mtDNA Mutation.Semantic proximity Read ↗

Leber’s hereditary optic neuropathy with late disease onset: clinical and molecular characteristics of 20 patientsSemantic proximity Read ↗

Childhood-onset Leber hereditary optic neuropathy.Semantic proximity Read ↗

Painful vision loss in Leber hereditary optic neuropathy with novel ND1 variant mimicking optic neuritis.Semantic proximity Read ↗

Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patientSemantic proximity Read ↗

Genotypic and phenotypic characteristics of Korean children with childhood-onset Leber's hereditary optic neuropathy.Semantic proximity Read ↗

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