A novel frameshift variant in the TSPAN12 gene causes autosomal dominant FEVR by Li Peng, Erkuan Dai, Haodong Xiao, Rulian Zhao, Yunqi He, Shujin Li, Mu Yang, Zhenglin Yang, Peiquan Zhao

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Refractive status and optical components in premature infants with and without retinopathy of prematurity: A 4- to 5-year cohort study by Xuanxuan Xie, Xuanxuan Xie, Xuanxuan Xie, Yang Wang, Yang Wang, Yang Wang, Rulian Zhao, Rulian Zhao, Rulian Zhao, Jing Yang, Jing Yang, Jing Yang, Xiaohui Zhu, Xiaohui Zhu, Xiaohui Zhu, Lijuan Ouyang, Lijuan Ouyang, Lijuan Ouyang, Ming Liu, Ming Liu, Ming Liu, Xinke Chen, Xinke Chen, Xinke Chen, Ning Ke, Ning Ke, Ning Ke, Yong Li, Yong Li, Yong Li, Lianhong Pi, Lianhong Pi, Lianhong Pi

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Defective EMC1 drives abnormal retinal angiogenesis via Wnt/β-catenin signaling and may be associated with the pathogenesis of familial exudative vitreoretinopathy by Shujin Li, Mu Yang, Rulian Zhao, Li Peng, Wenjing Liu, Xiaoyan Jiang, Yunqi He, Erkuan Dai, Lin Zhang, Yeming Yang, Yi Shi, Peiquan Zhao, Zhenglin Yang, Xianjun Zhu

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CTNND1 variants cause familial exudative vitreoretinopathy through the Wnt/cadherin axis by Mu Yang, Shujin Li, Li Huang, Rulian Zhao, Erkuan Dai, Xiaoyan Jiang, Yunqi He, Jinglin Lu, Li Peng, Wenjing Liu, Zhaotian Zhang, Dan Jiang, Yi Zhang, Zhilin Jiang, Yeming Yang, Peiquan Zhao, Xianjun Zhu, Xiaoyan Ding, Zhenglin Yang

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