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Molecular Vision|January 29, 2003
Mutation screening of patients with Leber Congenital Amaurosis or the enhanced S-Cone Syndrome reveals a lack of sequence variations in the NRL geneCeren Acar, Alan J Mears, Beverly M Yashar, et al.Genomics|April 2, 1998
Homozygosity and physical mapping of the autosomal recessive retinitis pigmentosa locus (RP14) on chromosome 6p21.3P Banerjee, C A Lewis, P W Kleyn, et al.Human Molecular Genetics|April 16, 2011
The Usher 1B protein, MYO7A, is required for normal localization and function of the visual retinoid cycle enzyme, RPE65Vanda S Lopes, Daniel Gibbs, Richard T Libby, et al.Genomics|August 29, 1998
Human rod monochromacy: linkage analysis and mapping of a cone photoreceptor expressed candidate gene on chromosome 2q11B Wissinger, H Jägle, S Kohl, et al.American Journal of Ophthalmology|February 19, 2017
Defining Outcomes for Clinical Trials of Leber Congenital Amaurosis Caused by GUCY2D MutationsSamuel G Jacobson, Artur V Cideciyan, Alexander Sumaroka, et al.Proceedings of the National Academy of Sciences of the United States of America|April 25, 2002
Naturally occurring rhodopsin mutation in the dog causes retinal dysfunction and degeneration mimicking human dominant retinitis pigmentosaJames W Kijas, Artur V Cideciyan, Tomas S Aleman, et al.Experimental Eye Research|February 5, 2002
Concentric retinitis pigmentosa: clinicopathologic correlationsA H Milam, E B De Castro, J E Smith, et al.Ophthalmology|March 8, 2003
Clinicopathologic effects of mutant GUCY2D in Leber congenital amaurosisAnn H Milam, Mark R Barakat, Nisha Gupta, et al.JAMA|August 14, 2008
Alcohol use and alcohol-related problems before and after military combat deploymentIsabel G Jacobson, Margaret A K Ryan, Tomoko I Hooper, et al.Investigative Ophthalmology & Visual Science|November 6, 1998
Retinal degenerations with truncation mutations in the cone-rod homeobox (CRX) geneS G Jacobson, A V Cideciyan, Y Huang, et al.Pageof 57