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Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 08/2016, Volume 57, Issue 10, pp. 3984 - 3995
Journal Article
Journal Article
Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 02/2017, Volume 58, Issue 2, pp. 821 - 832
Journal Article
Nature Genetics, ISSN 1061-4036, 2015, Volume 47, Issue 7, pp. 757 - 765
Journal Article
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 02/2019, Volume 129, Issue 2, pp. 513 - 515
Achromatopsia is an inherited retinal degeneration characterized by the loss of cone photoreceptor function. In this issue of the JCI, Moshiri et al.... 
MEDICINE, RESEARCH & EXPERIMENTAL | GENE-THERAPY | RESTORATION | VISION | CONE FUNCTION | MOUSE MODEL | Animal experimentation | Research | Gene mutations | Color blindness | Phenotypes | Phototransduction | Animals | Congenital diseases | Disease | Acetylcholine receptors | Retinal degeneration | Retina | Photoreceptors | Mutation | Gene therapy
Journal Article
Journal Article
Journal Article
Human Molecular Genetics, ISSN 0964-6906, 8/2011, Volume 20, Issue 16, pp. 3161 - 3175
Journal Article