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The British Journal of Ophthalmology|May 29, 1998
Multifocal electroretinography in patients with Stargardt's macular dystrophyU Kretschmann, M W Seeliger, K Ruether, et al.Cell Death Discovery|August 24, 2016
Efficacy of PARP inhibition in Pde6a mutant mouse models for retinitis pigmentosa depends on the quality and composition of individual human mutationsK Jiao, A Sahaboglu, E Zrenner, et al.Documenta Ophthalmologica. Advances in Ophthalmology|April 22, 2019
A case of X-linked retinoschisis with atypical fundus appearanceF Nasser, S Kohl, L Kuehlewein, et al.The European Journal of Neuroscience|March 28, 1998
Cloning, chromosomal localization and functional expression of the gene encoding the alpha-subunit of the cGMP-gated channel in human cone photoreceptorsB Wissinger, F Müller, I Weyand, et al.Investigative Ophthalmology & Visual Science|October 3, 2001
Slow and fast rod ERG pathways in patients with X-linked complete stationary night blindness carrying mutations in the NYX geneH P Scholl, H Langrová, C M Pusch, et al.Graefe'S Archive for Clinical and Experimental Ophthalmology = Albrecht Von Graefes Archiv Fur Klinische Und Experimentelle Ophthalmologie|October 29, 1997
Ocular findings in patients with autosomal dominant retinitis pigmentosa and Cys110Phe, Arg135Gly, and Gln344stop mutations of rhodopsinS Kremmer, A Eckstein, A Gal, et al.The British Journal of Ophthalmology|August 1, 1993
Ocular findings in a family with autosomal dominant retinitis pigmentosa and a frameshift mutation altering the carboxyl terminal sequence of rhodopsinE Apfelstedt-Sylla, M Kunisch, M Horn, et al.American Journal of Human Genetics|March 1, 1992
Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsinC J Weitz, Y Miyake, K Shinzato, et al.Human Genetics|September 12, 2000
Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1F K Jacobi, M Broghammer, K Pesch, et al.The British Journal of Ophthalmology|July 26, 2008
Cone and cone-rod dystrophy segregating in the same pedigree due to the same novel CRX gene mutationV B D Kitiratschky, D Nagy, T Zabel, et al.Pageof 26