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Article

Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patient

1 Oct 1998

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

Identifiers

PMID: 9849804
DOI: 10.1016/s0022-510x(98)00239-1

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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.

Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

Leber's Hereditary Optic Neuropathy (LHON) with 14484/ND6 mutation in a North African patientPMID 9849804Read ↗

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

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

Prevalence of primary mutations in Leber hereditary optic neuropathy: A five-year report from a tertiary eye care center in India.Semantic proximity Read ↗

Autosomal recessive Leber hereditary optic neuropathy, a new neuro-ophthalmo-genetic paradigm.Semantic proximity Read ↗

The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.Semantic proximity Read ↗

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

Frequency and spectrum of mitochondrial ND6 mutations in 1218 Han Chinese subjects with Leber's hereditary optic neuropathy.Semantic proximity Read ↗

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

[Study on three common mitochondrial DNA mutations in Leber's hereditary optic neuropathy].Semantic proximity Read ↗

Fifteen novel mutations in the mitochondrial NADH dehydrogenase subunit 1, 2, 3, 4, 4L, 5 and 6 genes from Iranian patients with Leber's hereditary optic neuropathy (LHON).Semantic proximity Read ↗

Leber's hereditary optic neuropathy (LHON) with mitochondrial ND4 gene mutation (11778) in a Thai patient.Semantic proximity Read ↗

Leber's Hereditary Optic Neuropathy is Associated with Compound Primary Mutations of Mitochondrial ND1 m.3635G > A and ND6 m.14502 T > C.Semantic proximity Read ↗

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