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Article

Choroidal neovascularization in patients with adult-onset foveomacular dystrophy caused by mutations in the RDS/peripherin gene.

Advances in experimental medicine and biology - 1 Jan 2006

Moshfeghi Darius M, Yang Zhenglin, Faulkner Nathan D, Karan Goutam, Thirumalaichary Sukanya, Pearson Erik, Zhao Yu, Tsai Thomas, Zhang Kang

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Share to Intermediate Filament Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 17249552
DOI: 10.1007/0-387-32442-9_6

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

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Choroidal neovascularization in patients with adult-onset foveomacular dystrophy caused by mutations in the RDS/peripherin gene.PMID 17249552Read ↗

A novel mutation in the RDS/Peripherin gene causes adult-onset foveomacular dystrophySemantic proximity Read ↗

Transgenic animal studies of human retinal disease caused by mutations in peripherin/rds.Semantic proximity Read ↗

Pattern dystrophy with high intrafamilial variability associated with Y141C mutation in the peripherin/RDS gene and successful treatment of subfoveal CNV related to multifocal pattern type with anti-VEGF (ranibizumab) intravitreal injections.Semantic proximity Read ↗

A novel RDS/peripherin gene mutation associated with diverse macular phenotypes.Semantic proximity Read ↗

Choroidal neovascularization in a patient with adult foveomacular dystrophy and a mutation in the retinal degeneration slow gene (Pro 210 Arg)Semantic proximity Read ↗

A novel peripherin/RDS mutation resulting in a retinal dystrophy with phenotypic variation.Semantic proximity Read ↗

Mutations in the human peripherin/RDS gene associated with autosomal dominant retinitis pigmentosa.Semantic proximity Read ↗

Adult vitelliform macular dystrophy is frequently associated with mutations in the peripherin/RDS gene.Semantic proximity Read ↗

The spectrum of retinal dystrophies caused by mutations in the peripherin/RDS gene.Semantic proximity Read ↗

Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigree.Semantic proximity Read ↗

Clinical Pathological Features and Current Animal Models of Type 3 Macular NeovascularizationSemantic proximity Read ↗

Polypoidal choroidal vasculopathy and neovascular age-related macular degeneration: same or different disease?Semantic proximity Read ↗

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