Long term follow-up of a family with GUCY2D dominant cone dystrophy
Author:
Publisher
Press of International Journal of Ophthalmology (IJO Press)
Subject
Ophthalmology
Link
http://www.ijo.cn/en_publish/2018/12/20181212.pdf
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. Phenotyping and genotyping inherited retinal diseases: Molecular genetics, clinical and imaging features, and therapeutics of macular dystrophies, cone and cone-rod dystrophies, rod-cone dystrophies, Leber congenital amaurosis, and cone dysfunction syndromes;Progress in Retinal and Eye Research;2024-05
2. Retinal Imaging Findings in Inherited Retinal Diseases;Journal of Clinical Medicine;2024-04-03
3. GUCY2D-Related Retinal Dystrophy with Autosomal Dominant Inheritance—A Multicenter Case Series and Review of Reported Data;Genes;2022-02-08
4. New Omics—Derived Perspectives on Retinal Dystrophies: Could Ion Channels-Encoding or Related Genes Act as Modifier of Pathological Phenotype?;International Journal of Molecular Sciences;2020-12-23
5. Variants at codon 838 in the GUCY2D gene result in different phenotypes of cone rod dystrophy;Ophthalmic Genetics;2020-08-18
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