Associated Papers
EARLY-ONSET OF FAMILIAL EXUDATIVE VITREORETINOPATHY: Clinical Characteristics, Management, and Outcomes.
Kitic N et al.
Retina (philadelphia, Pa.), 2024
Clinical characteristics and mutation spectrum in 33 Chinese families with familial exudative vitreoretinopathy.
Mao J et al.
Annals of Medicine, 2022
Ocular Features and Mutation Spectrum of Patients With Familial Exudative Vitreoretinopathy.
Tao T et al.
Investigative Ophthalmology & Visual Science, 2021
Familial Exudative Vitreoretinopathy-Related Disease-Causing Genes and Norrin/β-Catenin Signal Pathway: Structure, Function, and Mutation Spectrums.
Xiao H et al.
Journal of Ophthalmology, 2019
The characteristics of digenic familial exudative vitreoretinopathy.
Li Y et al.
Graefe's Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie, 2018
Identification of FZD4 and LRP5 mutations in 11 of 49 families with familial exudative vitreoretinopathy.
Yang H et al.
Molecular Vision, 2012
Select a paper to view details