Funder
VitreoRetinal Surgery Foundation
Research to Prevent Blindness
U.S. Department of Defense
NIH
Reference7 articles.
1. Mutations in LRP5, FZD4, TSPAN12, NDP, ZNF408, or KIF11 genes account for 38.7% of Chinese patients with familial exudative vitreoretinopathy;Rao;Invest Ophthalmol Vis Sci,2017
2. Complex genetics of familial exudative vitreoretinopathy and related pediatric retinal detachments;Kondo;Taiwan J Ophthalmol,2015
3. High prevalence of peripheral retinal vascular anomalies in family members of patients with familial exudative vitreoretinopathy;Kashani;Ophthalmology,2014
4. Genetic screening of Wnt signaling factors in advanced retinopathy of prematurity;Hiraoka;Mol Vis,2010
5. Genetic variants of FZD4 and LRP5 genes in patients with advanced retinopathy of prematurity;Kondo;Mol Vis,2013