Associated Papers
Whole-exome DNA sequencing in childhood anxiety disorders identifies rare de novo damaging coding variants.
Olfson E et al.
Depression and Anxiety, 2022
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
Spectrum of Variants in 389 Chinese Probands With Familial Exudative Vitreoretinopathy.
Li JK et al.
Investigative Ophthalmology & Visual Science, 2018
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
Mutations in LRP5,FZD4, TSPAN12, NDP, ZNF408, or KIF11 Genes Account for 38.7% of Chinese Patients With Familial Exudative Vitreoretinopathy.
Rao FQ et al.
Investigative Ophthalmology & Visual Science, 2017
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