Study of the involvement of the RGR, CRPB1, and CRB1 genes in the pathogenesis of autosomal recessive retinitis pigmentosa
Author:
Publisher
BMJ
Subject
Genetics(clinical),Genetics
Cited by 73 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. Human CRB1 and CRB2 form homo- and heteromeric protein complexes in the retina;Life Science Alliance;2024-04-03
2. The p.C759F Variant in <i>USH2A</i> Is a Pathogenic Mutation: Systematic Literature Review and Meta-Analysis of 667 Genotypes;Ophthalmic Research;2023-11-28
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4. CRB1-Related Retinal Dystrophies in a Cohort of 50 Patients: A Reappraisal in the Light of Specific Müller Cell and Photoreceptor CRB1 Isoforms;International Journal of Molecular Sciences;2021-11-23
5. Spectral-Domain Optical Coherence Tomography Analysis in Syndromic and Nonsyndromic Forms of Retinitis Pigmentosa due to <b><i>USH2A</i></b> Genetic Variants;Ophthalmic Research;2021-11-15
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