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JAMA Ophthalmology|August 31, 2013
Expanded clinical spectrum of enhanced S-cone syndromeSuzanne Yzer, Irene Barbazetto, Rando Allikmets, et al.Nature Genetics|July 14, 1998
Total colourblindness is caused by mutations in the gene encoding the alpha-subunit of the cone photoreceptor cGMP-gated cation channelS Kohl, T Marx, I Giddings, et al.Human Vaccines|April 3, 2008
Self-reported adverse health events following smallpox vaccination in a large prospective study of US military service membersTimothy S Wells, Cynthia A LeardMann, Tyler C Smith, et al.Molecular Therapy : the Journal of the American Society of Gene Therapy|November 16, 2001
Long-term protection of retinal structure but not function using RAAV.CNTF in animal models of retinitis pigmentosaF Q Liang, T S Aleman, N S Dejneka, et al.Human Mutation|July 20, 2001
Four novel mutations in the RPE65 gene in patients with Leber congenital amaurosisM J Simovich, B Miller, H Ezzeldin, et al.Noise & Health|January 21, 2015
Hearing loss associated with US military combat deploymentTimothy S Wells, Amber D Seelig, Margaret A K Ryan, et al.Proceedings of the National Academy of Sciences of the United States of America|June 17, 1998
Disease sequence from mutant rhodopsin allele to rod and cone photoreceptor degeneration in manA V Cideciyan, D C Hood, Y Huang, et al.Journal of the Optical Society of America. A, Optics, Image Science, and Vision|April 13, 2007
Reduced-illuminance autofluorescence imaging in ABCA4-associated retinal degenerationsArtur V Cideciyan, Malgorzata Swider, Tomas S Aleman, et al.International Journal of Molecular Sciences|November 14, 2019
Autosomal Dominant Retinitis Pigmentosa Due to Class B Rhodopsin Mutations: An Objective Outcome for Future Treatment TrialsAlexander Sumaroka, Artur V Cideciyan, Jason Charng, et al.Scientific Reports|August 3, 2017
CDHR1 mutations in retinal dystrophiesKatarina Stingl, Anja K Mayer, Pablo Llavona, et al.Pageof 57