Author:
Al Oreany Abdulaziz Abdulrahman,Al Hadlaq Abdulaziz,Schatz Patrik
Funder
Cronqvist Stiftelse of the Swedish Society of Medicine
The Foundation for the Visually Impaired in Skane County.
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Reference16 articles.
1. Zeitz C, Robson AG, Audo I (2015) Congenital stationary night blindness: an analysis and update of genotype-phenotype correlations and pathogenic mechanisms. Prog Retin Eye Res 45:58–110
2. Zeitz C, Forster U, Neidhardt J et al (2007) Night blindness-associated mutations in the ligand-binding, cysteine-rich, and intracellular domains of the metabotropic glutamate receptor 6 abolish protein trafficking. Hum Mutat 28:771–780
3. Schatz P, Preising M, Lorenz B et al (2010) Lack of autofluorescence in fundus albipunctatus associated with mutations in RDH5. Retina 30:1704–1713
4. Skorczyk-Werner A, Kocięcki J, Wawrocka A et al (2015) The first case of Oguchi disease, type 2 in a Polish patient with confirmed GRK1 gene mutation. Klin Ocz 117:27–30
5. Bijveld MM, Florijn RJ, Bergen AA et al (2013) Genotype and phenotype of 101 Dutch patients with congenital stationary night blindness. Ophthalmology 120:2072–2081
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