Genotype variant screening and phenotypic analysis of FBN1 in Chinese patients with isolated ectopia lentis
Author:
Affiliation:
1. State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat‑sen University, Guangzhou, Guangdong 510060, P.R. China
Publisher
Spandidos Publications
Subject
Cancer Research,Oncology,Genetics,Molecular Biology,Molecular Medicine,Biochemistry
Cited by 5 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Complications of high myopia: An update from clinical manifestations to underlying mechanisms;Advances in Ophthalmology Practice and Research;2024-08
2. Zonule-Associated Gene Variants in Isolated Ectopia Lentis and Glaucoma;Journal of Glaucoma;2023-03-20
3. Biallelic ADAMTSL4 variants in a Chinese cohort of congenital ectopia lentis: Implications for genotype–phenotype relationships;Human Mutation;2022-10-17
4. Cysteine Substitution and Calcium-Binding Mutations in FBN1 cbEGF-Like Domains Are Associated With Severe Ocular Involvement in Patients With Congenital Ectopia Lentis;Frontiers in Cell and Developmental Biology;2022-02-14
5. Mutation spectrum and genotype-phenotype correlations in Chinese congenital ectopia lentis patients;Experimental Eye Research;2021-06
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