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

Cognitive Impairment in Phenotypic Leber Hereditary Optic Neuropathy Caused by Mutation in Nuclear Gene NDUFAF5.

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

Chen Jieqiong, Wu Yidong, Yu Suqin, Wan Xiaolin, Gong Yuanyuan, Sun Xiaodong

Abstract excerpt

No abstract is available from the source.

Topics

Humans
Optic Atrophy, Hereditary, Leber
Mutation
Point Mutation
Cognitive Dysfunction
DNA, Mitochondrial
Methyltransferases
Mitochondrial Proteins

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 36580434
DOI: 10.1097/WNO.0000000000001760

Genes

NDUFAF5

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 31 Aug 2026.

Community interpretation

Discuss the evidence

Ask a question, add context or challenge an interpretation. Community activity is separate from scientific evidence strength.

0

discussions

0

replies

Citations encouraged

Claims remain attributable.

No discussion yet

Be the first to add a careful, cited interpretation.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Cognitive Impairment in Phenotypic Leber Hereditary Optic Neuropathy Caused by Mutation in Nuclear Gene NDUFAF5.PMID 36580434Read ↗

Visual Recovery in Leber Hereditary Optic Neuropathy From a Rare mt.14568 Mutation on ND6 Gene.Semantic proximity Read ↗

Nuclear DNA Mutation in KIF5A Causing Autosomal Dominant Phenotypic 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 ↗

Novel Mutations in the ND5 Gene Associated With Leber Hereditary Optic Neuropathy.Semantic proximity Read ↗

Novel MT-ND5 gene mutation identified in Leber's hereditary optic neuropathy patient using mitochondrial genome sequencing.Semantic proximity Read ↗

NDUFA-1 is not a nuclear modifier gene in Leber hereditary optic neuropathy.Semantic proximity Read ↗

Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation.Semantic proximity Read ↗

Recessive variants in mitochondrial complex I nuclear subunits are an underrated cause of optic atrophy.Semantic proximity Read ↗

Very low penetrance of Leber's hereditary optic neuropathy in five Han Chinese families carrying the ND1 G3460A mutation.Semantic proximity Read ↗

Severe Leber Hereditary Optic Neuropathy Plus Disease in a Middle-Aged Man.Semantic proximity Read ↗

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

Update on hereditary optic neuropathy.Semantic proximity Read ↗

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