Familial Exudative Vitreoretinopathy
Last Posted: Sep 29, 2021
- Severe exudative vitreoretinopathy as a common feature for CTNNB1, KIF11 and NDP variants plus sector degeneration for KIF11.
Yang Junxing, et al. American journal of ophthalmology 2021 9
- Novel FZD4 and LRP5 mutations in a small cohort of patients with familial exudative vitreoretinopathy (FEVR).
Carrera William et al. Ophthalmic genetics 2020 Dec 1-4
- Optical Coherence Tomography Angiography in Familial Exudative Vitreoretinopathy: Clinical Features and Phenotype-Genotype Correlation.
Chen Chonglin, et al. Investigative ophthalmology & visual science 2018 0 (15) 5726-5734
- Detection of FZD4, LRP5 and TSPAN12 Genes Variants in Malay Premature Babies with Retinopathy of Prematurity.
Mohd Khair Siti Zulaikha Nashwa, et al. Journal of ophthalmic & vision research 0 0 (2) 171-178
- Whole Exome Sequencing Analysis Identifies Mutations in LRP5 in Indian Families with Familial Exudative Vitreoretinopathy.
Zhang Lin, et al. Genetic testing and molecular biomarkers 2016 5
- Mutation spectrum of the Norrie disease pseudoglioma (NDP) gene in Indian patients with FEVR.
Musada Ganeswara Rao, et al. Molecular vision 2016 0 491-502
- Identification of novel KIF11 mutations in patients with familial exudative vitreoretinopathy and a phenotypic analysis.
Li Jia-Kai, et al. Scientific reports 2016 0 26564
- Identification and functional analysis of novel FZD4 mutations in Han Chinese with familial exudative vitreoretinopathy.
Fei Ping, et al. Scientific reports 2015 0 16120
- Novel mutations in the TSPAN12 gene in Chinese patients with familial exudative vitreoretinopathy.
Xu Yu, et al. Molecular vision 2014 0 1296-306
- Next-generation sequencing and novel variant determination in a cohort of 92 familial exudative vitreoretinopathy patients.
Salvo Jason, et al. Investigative ophthalmology & visual science 2015 3 (3) 1937-46
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