Gene therapy: perspectives from young adults with Leber’s congenital amaurosis
Author:
Funder
The R. Weksberg Grant
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
https://www.nature.com/articles/s41433-021-01763-z.pdf
Reference24 articles.
1. Astuti GDN, Bertelsen M, Preising MN, Ajmal M, Lorenz B, Faradz SMH, et al. Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in Denmark. Eur J Hum Genet. 2016;24:1071–9. https://doi.org/10.1038/ejhg.2015.241.
2. Walia S, Fishman GA, Jacobson SG, Aleman TS, Koenekoop RK, Traboulsi EI, et al. Visual acuity in patients with Leber’s congenital amaurosis and early childhood-onset retinitis pigmentosa. Ophthalmology. 2010;117:1190–8. https://doi.org/10.1016/j.ophtha.2009.09.056.
3. Heon E, Koenekoop R. Treatments for inherited retinal degenerations are coming to Canada: brief update on a new standard of care for inherited retinal degenerations. Can J Ophthalmol. 2021;56:e34–5. https://doi.org/10.1016/j.jcjo.2020.10.019.
4. Home - ClinicalTrials.gov n.d. https://clinicaltrials.gov/ (accessed March 19, 2021).
5. Morris MC, Besner D, Vazquez H, Nelson RM, Fischbach RL. Parental opinions about clinical research. J Pediatr 2007;151:532–7. 537.e1-5.
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