Ccdc66 null mutation causes retinal degeneration and dysfunction

A mouse M-opsin monochromat: Retinal cone photoreceptors have increased M-opsin expression when S-opsin is knocked out

(2011) Lauren L. Daniele et al.   VISION RESEARCH

The molecular basis of human retinal and vitreoretinal diseases

(2010) Wolfgang Berger et al.   PROGRESS IN RETINAL AND EYE RESEARCH

Electrophysiological deficits in the retina of the DBA/2J mouse

(2009) Joanna Harazny et al.   DOCUMENTA OPHTHALMOLOGICA

Prolonged illumination up-regulates arrestin and two guanylate cyclase activating proteins: a novel mechanism for light adaptation

(2009) Paolo Codega et al.   JOURNAL OF PHYSIOLOGY-LONDON

Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene

(2009) Gabriele Dekomien et al.   NEUROGENETICS

Naturally occurring animal models with outer retina phenotypes

(2009) Wolfgang Baehr et al.   VISION RESEARCH

Review and update: Current treatment trends for patients with retinitis pigmentosa

(2009) Kelly Shintani et al.   OPTOMETRY

Trafficking of Membrane-Associated Proteins to Cone Photoreceptor Outer Segments Requires the Chromophore 11-cis-Retinal

(2008) H. Zhang et al.   JOURNAL OF NEUROSCIENCE

Leber congenital amaurosis: Genes, proteins and disease mechanisms

(2008) Anneke I. den Hollander et al.   PROGRESS IN RETINAL AND EYE RESEARCH