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Article

An atypical Leber's hereditary optic neuropathy with the 11778 mutation.

The British journal of ophthalmology - 1 Nov 1993

Hotta Y, Hayakawa M, Fujiki K, Shinohara K, Sado K, Kanai A, Yanashima K

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Identifiers

PMID: 8280696
DOI: 10.1136/bjo.77.11.748
PMCID: PMC504642

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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An atypical Leber's hereditary optic neuropathy with the 11778 mutation.PMID 8280696Read ↗

The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.Semantic proximity Read ↗

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

Clinical features of Leber's hereditary optic neuropathy with the 11778 mitochondrial DNA mutation in Taiwanese patients.Semantic proximity Read ↗

A Novel Mitochondrial Mutation for Lebers Hereditary Optic Neuropathy Presenting With Vitamin B12 Deficiency.Semantic proximity Read ↗

Leber hereditary optic neuropathy harboring a rare m.12811 T>C mitochondrial DNA mutation.Semantic proximity Read ↗

A case of Leber hereditary optic neuropathy plus dystonia caused by G14459A mitochondrial mutation.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 hereditary optic neuropathy in 2 of 4 siblings with 11778 mtDNA mutation: clinical variability or effect of toxic environmental exposure?Semantic proximity Read ↗

Mitochondrial DNA mutation 14487T>C manifesting as Leber's hereditary optic neuropathy.Semantic proximity Read ↗

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

Mitochondrial genome variation in male LHON patients with the m.11778G > A mutation.Semantic proximity Read ↗

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