Gene therapy for RPE65-related retinal disease-Reference-Cited by-同舟云学术

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Gene therapy for RPE65-related retinal disease

Published:2018-10-18 Issue:6 Volume:39 Page:671-677
ISSN:1381-6810
Container-title:Ophthalmic Genetics
language:en
Short-container-title:Ophthalmic Genetics

Author:

Miraldi Utz Virginia¹²,Coussa Razek Georges³,Antaki Fares⁴,Traboulsi Elias I.³

Affiliation:

1. Cincinnati Children’s Hospital Medical Center, Abrahamson Pediatric Eye Institute, Cincinnati, OH, USA

2. Department of Ophthalmology, University of Cincinnati, Cincinnati, OH, USA

3. Cleveland Clinic, Cole Eye Institute, Cleveland, OH, USA

4. Department of Ophthalmology, Université de Montréal, Montreal, Quebec, Canada

Publisher

Informa UK Limited

Subject

Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/13816810.2018.1533027

Reference42 articles.

1. Vision in Leber Congenital Amaurosis

2. An overview of leber congenital amaurosis: a model to understand human retinal development

3. The Natural History of Leber's Congenital Amoaurosis

4. Molecular genetics of Leber congenital amaurosis

5. Clinical and Molecular Genetics of Leber's Congenital Amaurosis: A Multicenter Study of Italian Patients

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3. Preservation of retinal structure and function in two mouse models of inherited retinal degeneration by ONL1204, an inhibitor of the Fas receptor;Cell Death & Disease;2024-08-08

4. A novel homozygous missense mutation in the RPE65 gene in an Iranian family with retinitis pigmentosa;Gene Reports;2024-06

5. Nucleic acid delivery to retinal cells using lipopeptides as a potential tool towards ocular gene therapies;Journal of Colloid and Interface Science;2024-02

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