Mutation spectrum of the Norrie disease pseudoglioma (NDP) gene in Indian patients with FEVR

about

Mutation spectrum of the Norrie disease pseudoglioma (NDP) gene in Indian patients with FEVR

Item

http://www.wikidata.org/entity/Q36915072

description

2016 nî lūn-bûn

@nan

2016年の論文

@ja

2016年論文

@yue

2016年論文

@zh-hant

2016年論文

@zh-hk

2016年論文

@zh-mo

2016年論文

@zh-tw

2016年论文

@wuu

2016年论文

@zh

2016年论文

@zh-cn

name

Mutation spectrum of the Norri ...... e in Indian patients with FEVR

@en

type

Item

label

Mutation spectrum of the Norri ...... e in Indian patients with FEVR

@en

prefLabel

Mutation spectrum of the Norri ...... e in Indian patients with FEVR

@en

P1476

Mutation spectrum of the Norri ...... e in Indian patients with FEVR

@en

P2093

Anjli Hussain

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

Anupama Reddy Chururu

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

Ganeswara Rao Musada

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

Inderjeet Kaur

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

Pramod Reddy Gaddam

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

Subhabrata Chakrabarti

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

Subhadra Jalali

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

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

dbSNP: the NCBI database of genetic variation

A model for familial exudative vitreoretinopathy caused by LPR5 mutations

The Norrin/Frizzled4 signaling pathway in retinal vascular development and disease

P304

491-502

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

P31

scholarly article

P478

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

P577

2016-05-16T00:00:00Z

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

P698

27217716

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

P932

4872281

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