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Genetics in Medicine, ISSN 1098-3600, 10/2018, Volume 20, Issue 10, pp. 1206 - 1215
Journal Article
Progress in Retinal and Eye Research, ISSN 1350-9462, 03/2015, Volume 45, pp. 58 - 110
Congenital stationary night blindness (CSNB) refers to a group of genetically and clinically heterogeneous retinal disorders. Seventeen different genes with... 
Animal models | Prevalence | Fundus albipunctatus | Oguchi disease | Molecular genetics | Diagnostics | Pathophysiology | Protein function | Schubert-Bornschein | Congenital stationary night blindness (CSNB) | MELANOMA-ASSOCIATED RETINOPATHY | CALCIUM-DEPENDENT INACTIVATION | COMPOUND HETEROZYGOUS MUTATION | MIZUO-NAKAMURA PHENOMENON | ON-BIPOLAR CELLS | LEUCINE-RICH REPEAT | PRIMATE PHOTOPIC ELECTRORETINOGRAM | SCANNING LASER OPHTHALMOSCOPY | OPHTHALMOLOGY | 11-CIS-RETINOL DEHYDROGENASE GENE | RETINITIS PUNCTATA ALBESCENS | Humans | Eye Diseases, Hereditary - diagnosis | Myopia - diagnosis | Genetic Diseases, X-Linked - genetics | Myopia - therapy | Eye Proteins - genetics | Night Blindness - genetics | Night Blindness - therapy | Genetic Diseases, X-Linked - physiopathology | Disease Models, Animal | Electroretinography | Eye Diseases, Hereditary - physiopathology | Genetic Association Studies | Night Blindness - diagnosis | Genotype | Genetic Diseases, X-Linked - diagnosis | Eye Diseases, Hereditary - genetics | Myopia - genetics | Phenotype | Animals | Myopia - physiopathology | Night Blindness - physiopathology | Eye Diseases, Hereditary - therapy | Mutation | Genetic Diseases, X-Linked - therapy | Genetic Therapy - methods | Proteins | Genetic research | Genetic aspects | Genetic disorders | Analysis | Prevalence studies (Epidemiology)
Journal Article
British Journal of Ophthalmology, ISSN 0007-1161, 09/2017, Volume 101, Issue 9, pp. 1147 - 1154
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