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Acta Ophthalmologica, ISSN 1755-375X, 11/2017, Volume 95, Issue 7, pp. 717 - 726
Journal Article
Medicine, ISSN 0025-7974, 08/2018, Volume 97, Issue 32, p. e11499
Background:Cone-rod dystrophy (CORD) is an inherited, progressive retinal disorder with genetic and phenotypic heterogeneity. Here, we aimed to identify the... 
RETINOPATHIES | CRX mutation | VARIANTS | sanger sequencing | PHOTORECEPTOR | cosegregation analysis | MEDICINE, GENERAL & INTERNAL | LEBER CONGENITAL AMAUROSIS | cone-rod dystrophy | whole-exome sequencing | RETINITIS-PIGMENTOSA | HOMEOBOX GENE | TRANSCRIPTION FACTOR | Usage | Transcription factors | Nucleotide sequencing | Research | Gene mutations | DNA sequencing
Journal Article
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, ISSN 0146-0404, 07/2016, Volume 57, Issue 8, pp. 3780 - 3792
PURPOSE. Mutations in the retinal transcription factor cone-rod homeobox (CRX) gene result in severe dominant retinopathies. A large animal model, the Rdy cat,... 
RETINAL DEGENERATION | RDY CAT | OPTICAL COHERENCE TOMOGRAPHY | TRANSCRIPTIONAL NETWORK | CRX | LCA | ROD CONE DYSPLASIA | DE-NOVO MUTATIONS | retinopathy | cat | OPHTHALMOLOGY | animal model | HOMEOBOX GENE | RETINITIS-PIGMENTOSA | ANTISENSE OLIGONUCLEOTIDES | PHOTORECEPTOR GENE-EXPRESSION
Journal Article
Journal Article
Journal Article
Biochemical and Biophysical Research Communications, ISSN 0006-291X, 10/2012, Volume 426, Issue 4, pp. 498 - 503
Journal Article
Journal Article
Journal Article
Journal of Clinical Investigation, ISSN 0021-9738, 02/2014, Volume 124, Issue 2, pp. 631 - 643
Journal Article