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Article

A mutation in the Norrie disease gene (NDP) associated with familial exudative vitreoretinopathy.

Eye (London, England) - 1 Dec 2011

Chamney S, McLoone E, Willoughby C E

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Identifiers

PMID: 21960066
DOI: 10.1038/eye.2011.226
PMCID: PMC3234469

Genes

NDP

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Related research

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Research trail→

Click a neighbor to travelStep 1 · 12 closest

A mutation in the Norrie disease gene (NDP) associated with familial exudative vitreoretinopathy.PMID 21960066Read ↗

Novel Norrie disease gene mutations in Chinese patients with familial exudative vitreoretinopathy.Semantic proximity Read ↗

Novel mutation in the NDP gene associated with Norrie disease in a Chinese pedigree.Semantic proximity Read ↗

Identification of a recurrent missense mutation in the Norrie disease gene associated with a simplex case of exudative vitreoretinopathy.Semantic proximity Read ↗

Mutations in the <i>NDP</i> gene: contribution to Norrie disease, familial exudative vitreoretinopathy and retinopathy of prematuritySemantic proximity Read ↗

A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy.Semantic proximity Read ↗

Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity.Semantic proximity Read ↗

Missense mutation (Arg121Trp) in the Norrie disease gene associated with x-linked exudative vitreoretinopathy.Semantic proximity Read ↗

Retinal vascular abnormalities and dragged maculae in a carrier with a new NDP mutation (c.268delC) that caused severe Norrie disease in the proband.Semantic proximity Read ↗

Characterization of a novel heterozygous frameshift variant in NDP gene that causes familial exudative vitreoretinopathy in female patients.Semantic proximity Read ↗

A comprehensive functional analysis on the pathogenesis of novel TSPAN12 and NDP variants in familial exudative vitreoretinopathy.Semantic proximity Read ↗

Whole-Exome Sequencing Reveals Novel NDP Variants in X-Linked Familial Exudative Vitreoretinopathy.Semantic proximity Read ↗

Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP.Semantic proximity Read ↗

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