Associated Papers
Spectrum of Mutations in NDP Resulting in Ocular Disease; a Systematic Review.
Wawrzynski J et al.
Frontiers in Genetics, 2022
Structure and functional properties of Norrin mimic Wnt for signalling with Frizzled4, Lrp5/6, and proteoglycan.
Chang TH et al.
Elife, 2015
Norrie disease: first mutation report and prenatal diagnosis in an Indian family.
Ghosh M et al.
Indian Journal of Pediatrics, 2012
Overview of the mutation spectrum in familial exudative vitreoretinopathy and Norrie disease with identification of 21 novel variants in FZD4, LRP5, and NDP.
Nikopoulos K et al.
Human Mutation, 2010
Novel and recurrent NDP gene mutations in familial cases of Norrie disease and X-linked exudative vitreoretinopathy.
Pelcastre EL et al.
Clinical & Experimental Ophthalmology, 2010
Advanced bilateral persistent fetal vasculature associated with a novel mutation in the Norrie gene.
Dhingra S et al.
The British Journal of Ophthalmology, 2006
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