1. McCullough, K Tyler, Boye, Sanford L, Fajardo, Diego, Maeder, Morgan L, Boye, Shannon E. 2018. Somatic Gene Editing of GUCY2D by AAV-CRISPR/Cas9 Alters Retinal Structure and Function in Mouse and Macaque. In Human gene therapy, 30, 571-589. doi:10.1089/hum.2018.193. https://pubmed.ncbi.nlm.nih.gov/30358434/
2. Huang, Chu-Hsuan, Yang, Chung-May, Yang, Chang-Hao, Hou, Yu-Chih, Chen, Ta-Ching. 2021. Leber's Congenital Amaurosis: Current Concepts of Genotype-Phenotype Correlations. In Genes, 12, . doi:10.3390/genes12081261. https://pubmed.ncbi.nlm.nih.gov/34440435/
3. Sharon, Dror, Wimberg, Hanna, Kinarty, Yael, Koch, Karl-Wilhelm. 2017. Genotype-functional-phenotype correlations in photoreceptor guanylate cyclase (GC-E) encoded by GUCY2D. In Progress in retinal and eye research, 63, 69-91. doi:10.1016/j.preteyeres.2017.10.003. https://pubmed.ncbi.nlm.nih.gov/29061346/
4. Hahn, Leo C, Georgiou, Michalis, Almushattat, Hind, Michaelides, Michel, Boon, Camiel J F. 2022. The Natural History of Leber Congenital Amaurosis and Cone-Rod Dystrophy Associated with Variants in the GUCY2D Gene. In Ophthalmology. Retina, 6, 711-722. doi:10.1016/j.oret.2022.03.008. https://pubmed.ncbi.nlm.nih.gov/35314386/
5. Jacobson, Samuel G, Cideciyan, Artur V, Ho, Allen C, Dizhoor, Alexander M, Boye, Shannon E. 2021. Safety and improved efficacy signals following gene therapy in childhood blindness caused by GUCY2D mutations. In iScience, 24, 102409. doi:10.1016/j.isci.2021.102409. https://pubmed.ncbi.nlm.nih.gov/33997691/
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