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Human Molecular Genetics|August 8, 2018
Whole-exome sequencing revealed HKDC1 as a candidate gene associated with autosomal-recessive retinitis pigmentosaLin Zhang, Zixi Sun, Peiquan Zhao, et al.JCI Insight|June 14, 2022
CTNND1 variants cause familial exudative vitreoretinopathy through the Wnt/cadherin axisMu Yang, Shujin Li, Li Huang, et al.Pageof 5