Mutations in the human retinal degeneration slow gene in autosomal dominant retinitis pigmentosa

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Mutations within the Rhodopsin Gene in Patients with Autosomal Dominant Retinitis Pigmentosa Thaddeus P. Dryja, Terri L. McGee, Lauri B. Hahn, New England Journal of Medicine	1990	498
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Identification of a photoreceptor-specific mRNA encoded by the gene responsible for retinal degeneration slow (rds) Gabriel H. Travis, Miles B. Brennan, Patria E. Danielson, Nature Ocular DiseaseRetinaPhotoreceptor CellOphthalmologyGenetics	1989	399
The retinal degeneration slow (rds) gene product is a photoreceptor disc membrane-associated glycoprotein Gabriel H. Travis, J. Gregor Sutcliffe, Dean Bok Neuron Gene ProductOcular DiseaseSignal TransductionRetinaOphthalmology	1991	327
Photoreceptor peripherin is the normal product of the gene responsible for retinal degeneration in the rds mouse. G. E. Connell, R.A. Bascom, Laurie L. Molday, Proceedings of the National Academy of Sciences Ocular DiseaseGeneticsOptogeneticsGanglion CellRetina	1991	289
Development and degeneration of retina in <i>rds</i> mutant mice: Light microscopy S. Sanyal, Arno Ruiter, Richard K. Hawkins The Journal of Comparative Neurology	1980	240
A New H‐2‐Linked Mutation, <i>rds</i>, Causing Retinal Degeneration in the Mouse R. Van Nie, Dagmar Iványi, Peter Démant Tissue Antigens Genome InstabilityGenetic DisorderNew H‐2‐linked MutationGeneticsMolecular Biology	1978	192
Autosomal dominant retinitis pigmentosa: Four new mutations in rhodopsin, one of them in the retinal attachment site T J Keen, C.F. Inglehearn, Douglas H. Lester, Genomics New MutationsOcular DiseaseRetinaPhotoreceptor CellOphthalmology	1991	169

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