Late-Onset Retinal Degeneration Caused byC1QTNF5Mutation
Author:
Affiliation:
1. Scheie Eye Institute, University of Pennsylvania, Philadelphia
2. Medical Research Council Human Genetics Unit, Medical Research Council Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, Scotland
Publisher
American Medical Association (AMA)
Subject
Ophthalmology
Cited by 21 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. Treatment Strategy With Gene Editing for Late-Onset Retinal Degeneration Caused by a Founder Variant in C1QTNF5;Investigative Opthalmology & Visual Science;2023-12-22
2. Longitudinal Changes of Retinal Structure in Molecularly Confirmed C1QTNF5 Patients With Late-Onset Retinal Degeneration;Translational Vision Science & Technology;2023-12-12
3. MICROPERIMETRY IN FOVEAL-SPARING ATROPHIC LATE-ONSET RETINAL DEGENERATION;Retina;2023-09
4. Anterior segment phenotypic changes in late-onset retinal degeneration with Ser163Arg mutation in CTRP5/C1QTNF5;Graefe's Archive for Clinical and Experimental Ophthalmology;2023-04-12
5. Distinct Phenotypic Consequences of Pathogenic Mutants Associated with Late-Onset Retinal Degeneration;The American Journal of Pathology;2022-10
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