Dominant optic atrophy. Refining the clinical diagnostic criteria in light of genetic linkage studies (Q28295091)

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M J Seller

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J T Behnam

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M A Burdon

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D J Spalton

Dominant optic atrophy mapped to chromosome 3q region. II. Clinical and epidemiological aspects

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language of work or name

English

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publication date

January 1999

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published in

Ophthalmology

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volume

106

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issue

1

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page(s)

123-8

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cites work

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Diagnostic criteria in cominantly inherited juvenile optic atrophy. A report of three new families

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Dominant optic atrophy. The clinical profile

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Autosomal dominant optic atrophy. A spectrum of disability.

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Histopathology of eye, optic nerve and brain in a case of dominant optic atrophy

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A Clinicopathologic Study of Autosomal Dominant Optic Atrophy

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Dominant optic atrophy (OPA1) mapped to chromosome 3q region. I. Linkage analysis.

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Genetic refinement of dominant optic atrophy (OPA1) locus to within a 2 cM interval of chromosome 3q

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No evidence of genetic heterogeneity in dominant optic atrophy

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Clinical and genetic analysis of a family affected with dominant optic atrophy (OPA1)

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Electrophysiology and colour perimetry in dominant infantile optic atrophy

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Clinical heterogeneity of dominant optic atrophy: the contribution of visual function investigations to diagnosis

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Hereditary optic atrophy. An autosomal dominant with incomplete penetrance

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Construction of multilocus genetic linkage maps in humans

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Clinically detectable nerve fiber atrophy precedes the onset of glaucomatous field loss

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Optic nerve damage in human glaucoma. III. Quantitative correlation of nerve fiber loss and visual field defect in glaucoma, ischemic neuropathy, papilledema, and toxic neuropathy

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Visual prognosis in autosomal dominant optic atrophy (Kjer type)

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