Literature DB >> 21960066

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

S Chamney, E McLoone, C E Willoughby.   

Abstract

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Year:  2011        PMID： 21960066      PMCID： PMC3234469          DOI： 10.1038/eye.2011.226

Source DB:  PubMed          Journal:  Eye (Lond)        ISSN： 0950-222X            Impact factor:   3.775


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  2 in total

1.  NDP gene mutations in 14 French families with Norrie disease.

Authors:  Ghislaine Royer; Sylvain Hanein; Valérie Raclin; Nadine Gigarel; Jean-Michel Rozet; Arnold Munnich; Julie Steffann; Jean-Louis Dufier; Josseline Kaplan; Jean-Paul Bonnefont
Journal:  Hum Mutat       Date:  2003-12       Impact factor: 4.878

2.  Genotype-phenotype variations in five Spanish families with Norrie disease or X-linked FEVR.

Authors:  Rosa Riveiro-Alvarez; Maria José Trujillo-Tiebas; Ascension Gimenez-Pardo; Maria Garcia-Hoyos; Diego Cantalapiedra; Isabel Lorda-Sanchez; Marta Rodriguez de Alba; Carmen Ramos; Carmen Ayuso
Journal:  Mol Vis       Date:  2005-09-02       Impact factor: 2.367
  2 in total
  2 in total

Review 1.  Wnt signaling pathway in retinal vascularization.

Authors:  Kimberly A Drenser
Journal:  Eye Brain       Date:  2016-08-09

2.  Targeted next-generation sequencing analysis identifies novel mutations in families with severe familial exudative vitreoretinopathy.

Authors:  Xiao-Yan Huang; Hong Zhuang; Ji-Hong Wu; Jian-Kang Li; Fang-Yuan Hu; Yu Zheng; Laurent Christian Asker M Tellier; Sheng-Hai Zhang; Feng-Juan Gao; Jian-Guo Zhang; Ge-Zhi Xu
Journal:  Mol Vis       Date:  2017-08-23       Impact factor: 2.367
  2 in total

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