Leber congenital amaurosis: Genes, proteins and disease mechanisms
Author:
Publisher
Elsevier BV
Subject
Sensory Systems,Ophthalmology
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1. Optical coherence tomography in children with inherited retinal disease;Clinical and Experimental Optometry;2024-01-22
2. The Clinical Findings, Pathogenic Variants, and Gene Therapy Qualifications Found in a Leber Congenital Amaurosis Phenotypic Spectrum Patient Cohort;International Journal of Molecular Sciences;2024-01-19
3. RNA-Seq Analysis of Trans-Differentiated ARPE-19 Cells Transduced by AAV9-AIPL1 Vectors;International Journal of Molecular Sciences;2023-12-22
4. A novel pathogenic CRB1 variant presenting as Leber Congenital Amaurosis 8 and evaluation of gene editing feasibility;Documenta Ophthalmologica;2023-10-07
5. Multi-luminance mobility testing after gene therapy in the context of retinal functional diagnostics;Graefe's Archive for Clinical and Experimental Ophthalmology;2023-09-28
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