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

Three subgroups of patients from the United Kingdom with Leber hereditary optic neuropathy.

Eye (London, England) - 1 Jan 1994

Mackey D A

Abstract excerpt

Variations in classic Leber hereditary optic neuropathy (LHON) include recovery of vision and association with other neurological abnormalities. Sixteen multi-generational Australian families originating from the United Kingdom with LHON were studied by the one examiner, using the same protocol....

Topics

Adult
Age Factors
Australia
Blindness
Color Vision Defects
DNA, Mitochondrial
Female
Humans
Male
Optic Atrophies, Hereditary
Phenotype
Point Mutation
United Kingdom

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Visual Fields

Source

Identifiers

PMID: 7821467
DOI: 10.1038/eye.1994.102

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 30 Aug 2026. Prepared record publication-7821467-2026-08-30.1. Manifest publication-graph-cohort-2026-08-30.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 30 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 · 10 closest

Three subgroups of patients from the United Kingdom with Leber hereditary optic neuropathy.PMID 7821467Read ↗

Leber hereditary optic neuropathy in Australia.Semantic proximity Read ↗

Lightning strikes twice: Leber hereditary optic neuropathy families with two pathogenic mtDNA mutations.Semantic proximity Read ↗

An example of Leber hereditary optic neuropathy not involving a mutation in the mitochondrial ND4 gene.Semantic proximity Read ↗

Remarkable recovery of visual function in a patient with Leber's optic neuropathy and multiple mutations of mitochondrial DNA.Semantic proximity Read ↗

Colour vision defects in asymptomatic carriers of the Leber's hereditary optic neuropathy (LHON) mtDNA 11778 mutation from a large Brazilian LHON pedigree: a case-control study.Semantic proximity Read ↗

Identical twins who are discordant for Leber's hereditary optic neuropathy.Semantic proximity Read ↗

Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.Semantic proximity Read ↗

Identical twins no longer discordant for Leber's hereditary optic neuropathy.Semantic proximity Read ↗

On the many faces of Leber hereditary optic neuropathy.Semantic proximity Read ↗

Visual recovery in patients with Leber's hereditary optic neuropathy and the 11778 mutation.Semantic proximity Read ↗

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