(Q28142455)

English

Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14

scientific article (publication date: April 1999)

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scholarly article

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Autosomal dominant Stargardt-like macular dystrophy: I. Clinical characterization, longitudinal follow-up, and evidence for a common ancestry in families linked to chromosome 6q14 (English)

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author name string

A O Edwards

1

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A Miedziak

2

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T Vrabec

3

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J Verhoeven

4

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T S Acott

5

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R G Weleber

6

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L A Donoso

7

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language of work or name

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publication date

April 1999

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American Journal of Ophthalmology

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127

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4

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426-35

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A photoreceptor cell-specific ATP-binding transporter gene (ABCR) is mutated in recessive Stargardt macular dystrophy

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Clinical and genetic heterogeneity in retinitis pigmentosa

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Mapping of autosomal dominant cone degeneration to chromosome 17p

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X-shaped macular dystrophy with flavimaculatus flecks

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North Carolina macular dystrophy and central areolar pigment epithelial dystrophy. One family, one disease

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Sorsby's fundus dystrophy in the British Isles: demonstration of a striking founder effect by microsatellite-generated haplotypes

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Autosomal-dominant fundus flavimaculatus. Clinicopathologic correlation

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10.1016/S0002-9394(98)00331-6

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