Ultra-widefield fundus autofluorescence imaging in patients with autosomal recessive retinitis pigmentosa reveals a genotype–phenotype correlation
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology
Link
https://link.springer.com/content/pdf/10.1007/s00417-022-05683-w.pdf
Reference20 articles.
1. Haim M (2002) The epidemiology of retinitis pigmentosa in Denmark. Acta Ophthalmol Scand 80:1–34. https://doi.org/10.1046/j.1395-3907.2002.00001.x
2. Grøndahl J (1987) Estimation of prognosis and prevalence of retinitis pigmentosa and Usher syndrome in Norway. Clin Genet 31:255–264. https://doi.org/10.1111/j.1399-0004.1987.tb02804.x
3. Bunker CH, Berson EL, Bromley WC, Hayes RP, Roderick TH (1984) Prevalence of retinitis pigmentosa in maine. Am J Ophthalmol 97:357–365. https://doi.org/10.1016/0002-9394(84)90636-6
4. Sharon D, Banin E (2015) Nonsyndromic retinitis pigmentosa is highly prevalent in the Jerusalem region with a high frequency of founder mutations. Mol Vis 21:783–792
5. Daiger SP, Sullivan LS, Bowne SJ (2016) RetNet, the Retinal Information Network.
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