Novel mutations in FZD4 and phenotype-genotype correlation in Chinese patients with familial exudative vitreoretinopathy

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Molecular genetics and targeted therapy of WNT-related human diseases (Review).Clinical and next-generation sequencing findings in a Chinese family exhibiting severe familial exudative vitreoretinopathy.

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Novel mutations in FZD4 and phenotype-genotype correlation in Chinese patients with familial exudative vitreoretinopathy

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http://www.wikidata.org/entity/Q37142456

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article científic

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article scientifique

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articolo scientifico

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artigo científico

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bilimsel makale

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scientific article published on 30 July 2016

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vedecký článok

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vetenskaplig artikel

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videnskabelig artikel

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vědecký článek

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Novel mutations in FZD4 and ph ...... al exudative vitreoretinopathy

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Novel mutations in FZD4 and ph ...... l exudative vitreoretinopathy.

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Novel mutations in FZD4 and ph ...... al exudative vitreoretinopathy

@en

Novel mutations in FZD4 and ph ...... l exudative vitreoretinopathy.

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Novel mutations in FZD4 and ph ...... al exudative vitreoretinopathy

@en

Novel mutations in FZD4 and ph ...... l exudative vitreoretinopathy.

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Novel mutations in FZD4 and ph ...... al exudative vitreoretinopathy

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Andina Hu

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Jiaqing Li

http://www.w3.org/2001/XMLSchema#string

Lin Lu

http://www.w3.org/2001/XMLSchema#string

Miao Tang

http://www.w3.org/2001/XMLSchema#string

Xiaoyan Ding

http://www.w3.org/2001/XMLSchema#string

Yu Yang

http://www.w3.org/2001/XMLSchema#string

Zijing Li

http://www.w3.org/2001/XMLSchema#string

Zongyi Zhan

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P2860

ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature

Autosomal recessive familial exudative vitreoretinopathy is associated with mutations in LRP5.

Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy

Mutations in LRP5 or FZD4 underlie the common familial exudative vitreoretinopathy locus on chromosome 11q.

Vascular development in the retina and inner ear: control by Norrin and Frizzled-4, a high-affinity ligand-receptor pair

A mutation in the Norrie disease gene (NDP) associated with X-linked familial exudative vitreoretinopathy

TSPAN12 regulates retinal vascular development by promoting Norrin- but not Wnt-induced FZD4/beta-catenin signaling

Insights into Wnt binding and signalling from the structures of two Frizzled cysteine-rich domains

Familial exudative vitreoretinopathy. Results of surgical management.

Next-generation sequencing of a 40 Mb linkage interval reveals TSPAN12 mutations in patients with familial exudative vitreoretinopathy.

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scholarly article

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Miner Yuan

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2016-07-30T00:00:00Z

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Novel mutations in FZD4 and phenotype-genotype correlation in Chinese patients with familial exudative vitreoretinopathy

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P2860

P2860

Novel mutations in FZD4 and phenotype-genotype correlation in Chinese patients with familial exudative vitreoretinopathy

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