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Article

Stargardt disease: linkage to the ABCR gene region on 1p21-p22 in Scandinavian families.

Acta ophthalmologica Scandinavica - 1 Dec 1998

Arnell H, Mäntyjärvi M, Tuppurainen K, Andréasson S, Dahl N

Abstract excerpt

UNLABELLED: Stargardt disease (STGD) or fundus flavimaculatus (FFM) is one of the most frequent causes of macular degeneration in childhood. The disease is inherited as an autosomal recessive trait and the corresponding gene has been localized to chromosome 1p21-22 and subsequently identified as the ATP-binding cassette transporter (ABCR) gene. PURPOSE: To characterize Finnish and Swedish STGD families...

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Identifiers

PMID: 9881544
DOI: 10.1034/j.1600-0420.1998.760602.x

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Stargardt disease: linkage to the ABCR gene region on 1p21-p22 in Scandinavian families.PMID 9881544Read ↗

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A new locus for autosomal dominant stargardt-like disease maps to chromosome 4.Semantic proximity Read ↗

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The ABCR gene in recessive and dominant Stargardt diseases: a genetic pathway in macular degeneration.Semantic proximity Read ↗

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