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Investigative Ophthalmology and Visual Science, ISSN 0146-0404, 2017, Volume 58, Issue 10, pp. 3840 - 3850
PURPOSE. To define the phenotype of C2orf71 associated retinopathy and to present novel mutations in this gene. METHODS. A retrospective multicenter study of... 
Outer retinal tabulation | Phenotype | Retinitis pigmentosa | C2orf71 gene | phenotype | GENE | VISUAL FUNCTION | FAMILIES | outer retinal tubulation | DISEASE | retinitis pigmentosa | OPHTHALMOLOGY | COHORT | PHENOTYPE ASSESSMENT | Index Medicus
Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 9675 - 10
Journal Article
Animal Genetics, ISSN 0268-9146, 06/2018, Volume 49, Issue 3, pp. 237 - 241
Progressive retinal atrophy ( PRA ) is a common cause of blindness in many dog breeds. It is most often inherited as a simple Mendelian trait, but great... 
retinitis pigmentosa | C2orf71 | blindness | C17H2orf71 | PRA | AGRICULTURE, DAIRY & ANIMAL SCIENCE | DNA | CONE DEGENERATION | GENES | GENETICS & HEREDITY | BREED | RETINITIS-PIGMENTOSA | Genomics | Genetic aspects | Blindness | Atrophy | Dogs | Retinal degeneration | Insertion | Retina | Genomes | Mutation | Gene sequencing | Index Medicus
Journal Article
HUMAN MUTATION, ISSN 1059-7794, 04/2011, Volume 32, Issue 4, pp. E2091 - E2103
Autosomal-recessive retinitis pigmentosa (arRP) is a genetically heterogeneous group of disorders to which a novel gene, C2orf71, was recently associated. The... 
USH2A GENE | EYS GENE | SERVER | GENETICS & HEREDITY | RECESSIVE RETINITIS-PIGMENTOSA | Rod-cone dystrophies | Autosomal-recessive retinitis pigmentosa | C2orf71
Journal Article
Human Mutation, ISSN 1059-7794, 04/2011, Volume 32, Issue 4, pp. E2091 - E2103
Autosomal‐recessive retinitis pigmentosa (arRP) is a genetically heterogeneous group of disorders to which a novel gene, C2orf71 , was recently associated. The... 
Autosomal‐recessive retinitis pigmentosa | Rod‐cone dystrophies | C2orf71 | Rod-cone dystrophies | Autosomal-recessive retinitis pigmentosa | Genes, Recessive - genetics | Pedigree | Humans | Retinitis Pigmentosa - genetics | Adult | Female | Heterozygote | Male | Eye Proteins - genetics | Mutation | France | Index Medicus
Journal Article
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