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Visual Neuroscience|April 7, 2006
The nob2 mouse, a null mutation in Cacna1f: anatomical and functional abnormalities in the outer retina and their consequences on ganglion cell visual responsesBo Chang, John R Heckenlively, Philippa R Bayley, et al.The Journal of Physiology|August 9, 2008
Allelic variance between GRM6 mutants, Grm6nob3 and Grm6nob4 results in differences in retinal ganglion cell visual responsesDennis M Maddox, Kirstan A Vessey, Gary L Yarbrough, et al.American Journal of Human Genetics|June 21, 2008
Infantile spasms is associated with deletion of the MAGI2 gene on chromosome 7q11.23-q21.11Christian R Marshall, Edwin J Young, Ariel M Pani, et al.American Journal of Human Genetics|February 14, 2012
GPR179 is required for depolarizing bipolar cell function and is mutated in autosomal-recessive complete congenital stationary night blindnessNeal S Peachey, Thomas A Ray, Ralph Florijn, et al.Biorxiv : the Preprint Server for Biology|October 3, 2025
RHO1-2 meganuclease gene editing targets human P23H rhodopsin-induced retinitis pigmentosa to rejuvenate rods and maintain conesArchana Jalligampala, Jacob M Young, Jack Feist, et al.American Journal of Human Genetics|December 1, 2014
Mutations in RAB39B cause X-linked intellectual disability and early-onset Parkinson disease with α-synuclein pathologyGabrielle R Wilson, Joe C H Sim, Catriona McLean, et al.Pageof 7