Associated Papers
Clinical and genetical features of probands and affected family members with familial exudative vitreoretinopathy in a large Chinese cohort.
Wang S et al.
The British Journal of Ophthalmology, 2021
Variable reduction in Norrin signaling activity caused by novel mutations in FZD4 identified in patients with familial exudative vitreoretinopathy.
Tian T et al.
Molecular Vision, 2019
Spectrum of Variants in 389 Chinese Probands With Familial Exudative Vitreoretinopathy.
Li JK et al.
Investigative Ophthalmology & Visual Science, 2018
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