Rod and Cone Function in Patients with KCNV2 Retinopathy
Author:
Publisher
Public Library of Science (PLoS)
Subject
Multidisciplinary
Cited by 27 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. Novel and Previously Known Mutations of the KCNV2 Gene Cause Various Variants of the Clinical Course of Cone Dystrophy with Supernormal Rod Response in Children;Journal of Clinical Medicine;2024-08-06
2. Natural history and biomarkers of KCNV2‐associated retinopathy;Clinical & Experimental Ophthalmology;2024-03-05
3. KCNV2-associated retinopathy: genotype–phenotype correlations –KCNV2study group report 3;British Journal of Ophthalmology;2023-10-18
4. Genetic and Clinical Profile of Retinopathies Due to Disease-Causing Variants in Leber Congenital Amaurosis (LCA)-Associated Genes in a Large German Cohort;International Journal of Molecular Sciences;2023-05-17
5. KCNV2-Associated Retinopathy: Detailed Retinal Phenotype and Structural Endpoints—KCNV2 Study Group Report 2;American Journal of Ophthalmology;2021-10
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