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Article

Detection of the mtDNA 14484 mutation on an African-specific haplotype: implications about its role in causing Leber hereditary optic neuropathy.

American journal of human genetics - 1 Jul 1996

Torroni A, Carelli V, Petrozzi M, Terracina M, Barboni P, Malpassi P, Wallace D C, Scozzari R

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Share to Africa
Share to DNA, Mitochondrial
Share to Evolution, Molecular
Share to Haplotypes

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Optic Atrophies, Hereditary

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Identifiers

PMID: 8659531
PMCID: PMC1915130

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

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Detection of the mtDNA 14484 mutation on an African-specific haplotype: implications about its role in causing Leber hereditary optic neuropathy.PMID 8659531Read ↗

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

De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy.Semantic proximity Read ↗

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Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.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 ↗

Whole Mitochondrial Genome Analysis in Serbian Cases of Leber's Hereditary Optic Neuropathy.Semantic proximity Read ↗

Mitochondrial DNA sequence variation and haplogroup distribution in Chinese patients with LHON and m.14484T>C.Semantic proximity Read ↗

Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.Semantic proximity Read ↗

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

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

m.3635G>A mutation as a cause of Leber hereditary optic neuropathy.Semantic proximity Read ↗

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