Ocular Findings in Patients With Autosomal Dominant Retinitis Pigmentosa and a Rhodopsin Gene Defect (Pro-23-His)
Author:
Publisher
American Medical Association (AMA)
Subject
Ophthalmology
Cited by 192 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. Clinical and genetic features of Koreans with retinitis pigmentosa associated with mutations in rhodopsin;Frontiers in Genetics;2023-08-29
2. Pre- and postsynaptic alterations in the visual cortex of the P23H-1 retinal degeneration rat model;Frontiers in Neuroanatomy;2022-10-13
3. Intravitreal and subretinal syngeneic bone marrow mononuclear stem cell transplantation improves photoreceptor survival but does not ameliorate retinal function in two rat models of retinal degeneration;Acta Ophthalmologica;2022-05-05
4. Beyond Sector Retinitis Pigmentosa: Expanding the Phenotype and Natural History of the Rhodopsin Gene Codon 106 Mutation (Gly-to-Arg) in Autosomal Dominant Retinitis Pigmentosa;Genes;2021-11-23
5. Transcriptional Profiling Identifies Upregulation of Neuroprotective Pathways in Retinitis Pigmentosa;International Journal of Molecular Sciences;2021-06-11
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