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Article

A new phenotype of macular dystrophy associated with a mitochondrial A3243G mutation.

Clinical & experimental ophthalmology - 1 Jan 2000

Sivaprasad Sobha, Kung Boom Ting, Robson Anthony G, Black Graeme, Webster Andrew R, Bird Alan, Egan Catherine

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 18290960
DOI: 10.1111/j.1442-9071.2007.01656.x

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A new phenotype of macular dystrophy associated with a mitochondrial A3243G mutation.PMID 18290960Read ↗

Macular dystrophy associated with the mitochondrial DNA A3243G mutation: pericentral pigment deposits or atrophy? Report of two cases and review of the literatureSemantic proximity Read ↗

The Spectrum of Maculopathy in Mitochondrial DNA A3243G Mutation: A Case Series of Six Patients.Semantic proximity Read ↗

Macular dystrophy with associated retinitis pigmentosa-1 like 1 genetic mutation.Semantic proximity Read ↗

Retinal involvement in m.3243A>G carriers.Semantic proximity Read ↗

Molecular genetics of macular dystrophies.Semantic proximity Read ↗

Diagnosis of maternally inherited diabetes and deafness (mitochondrial A3243G mutation) based on funduscopic appearance in an asymptomatic patient.Semantic proximity Read ↗

Macular Dystrophy Associated With the A3243G Mitochondrial DNA MutationSemantic proximity Read ↗

Exudative retinopathy in a girl with Alström syndrome due to a novel mutation.Semantic proximity Read ↗

Two sisters with macular dystrophy caused by the 3243A>G mitochondrial DNA mutation.Semantic proximity Read ↗

Protean phenotypic features of the A3243G mitochondrial DNA mutation.Semantic proximity Read ↗

Bringing the genetics of macular degeneration into focus.Semantic proximity Read ↗

Gene symbol: ABCA4. Disease: Macular dystrophy.Semantic proximity Read ↗

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