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Article

Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCR

1 Jan 1998

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Share to Photoreceptor and optogenetics research
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 9425888
DOI: 10.1038/ng0198-11

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Retinitis pigmentosa caused by a homozygous mutation in the Stargardt disease gene ABCRPMID 9425888Read ↗

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Analysis of the stargardt disease gene (ABCR) in age-related macular degeneration☆Semantic proximity Read ↗

Late-onset Stargardt disease is associated with missense mutations that map outside known functional regions of ABCR ( ABCA4 )Semantic proximity Read ↗

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A photoreceptor cell-specific ATP-binding trans- porter gene (ABCR) is mutated in recessive Star- gardt macular dystrophy.Semantic proximity Read ↗

Mechanistic Studies of ABCR, the ABC Transporter in Photoreceptor Outer Segments Responsible for Autosomal Recessive Stargardt DiseaseSemantic proximity Read ↗

Stargardt’s Disease: Molecular Pathogenesis and Current Therapeutic LandscapeSemantic proximity Read ↗

Molecular analysis of the ABCA4 gene in Turkish patients with Stargardt disease and retinitis pigmentosa.Semantic proximity Read ↗

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[Clinical and genetic aspects of ABCA4-associated inherited retinal diseases].Semantic proximity Read ↗

Spectrum of ABCR gene mutations in autosomal recessive macular dystrophies.Semantic proximity Read ↗

Pathogenic Mechanisms Underlying Stargardt Macular Degeneration Linked to Mutations in the Transmembrane Domains of ABCA4Semantic proximity Read ↗

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