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Mutation spectrum in a cohort with familial exudative vitreoretinopathy.
Qu N, Li W, Han DM, Gao JY, Yang ZT, Jiang L, Liu TB, Chen YX, Jiang XS, Zhou L, Wu JH, Huang X. Qu N, et al. Among authors: li w. Mol Genet Genomic Med. 2022 Sep;10(9):e2021. doi: 10.1002/mgg3.2021. Epub 2022 Jul 25. Mol Genet Genomic Med. 2022. PMID: 35876299 Free PMC article.
Prevalence and genetic-phenotypic characteristics of patients with USH2A mutations in a large cohort of Chinese patients with inherited retinal disease.
Gao FJ, Wang DD, Chen F, Sun HX, Hu FY, Xu P, Li J, Liu W, Qi YH, Li W, Wang M, Zhang S, Xu GZ, Chang Q, Wu JH. Gao FJ, et al. Among authors: li j, li w. Br J Ophthalmol. 2021 Jan;105(1):87-92. doi: 10.1136/bjophthalmol-2020-315878. Epub 2020 Mar 18. Br J Ophthalmol. 2021. PMID: 32188678 Free PMC article.
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