Gene Augmentation for Autosomal Dominant CRX-Associated Retinopathies
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Publisher
Springer International Publishing
Link
https://link.springer.com/content/pdf/10.1007/978-3-031-27681-1_21
Reference44 articles.
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2. Chen S, et al. Crx, a novel Otx-like paired-homeodomain protein, binds to and Transactivates photoreceptor cell-specific genes. Neuron. 1997;19(5):1017–30.
3. Tran NM, et al. Mechanistically distinct mouse models for CRX-associated retinopathy. PLoS Genet. 2014;10(2):e1004111.
4. Hull S, et al. The phenotypic variability of retinal dystrophies associated with mutations in CRX, with report of a novel macular dystrophy phenotype. Invest Ophthalmol Vis Sci. 2014;55(10):6934–44.
5. Sohocki MM, et al. Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies. Hum Mutat. 2001;17(1):42–51.
Cited by 2 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. Transcriptional precision in photoreceptor development and diseases – Lessons from 25 years of CRX research;Frontiers in Cellular Neuroscience;2024-02-13
2. The New Era of Therapeutic Strategies for the Treatment of Retinitis Pigmentosa: A Narrative Review of Pathomolecular Mechanisms for the Development of Cell-Based Therapies;Biomedicines;2023-09-28
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