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Research Article

Prevalence and Diagnostic Spectrum of Generalized Retinal Dystrophy in Danish Children

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Pages 164-169 | Received 31 Jul 2012, Accepted 22 Nov 2012, Published online: 10 May 2013

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Read on this site (4)

Rachael C. Heath Jeffery, Syed Aqif Mukhtar, Ian L. McAllister, William H. Morgan, David A. Mackey & Fred K. Chen. (2021) Inherited retinal diseases are the most common cause of blindness in the working-age population in Australia. Ophthalmic Genetics 42:4, pages 431-439.
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W. Bailey Glen$suffix/text()$suffix/text(), M. Millicent W. Peterseim, Ramses Badilla, Iya Znoyko, Andre Bourg, Robert Wilson, Gary Hardiman, Daynna Wolff & Joaquin Martinez. (2019) A high prevalence of biallelic RPE65 mutations in Costa Rican children with Leber congenital amaurosis and early-onset retinal dystrophy. Ophthalmic Genetics 40:2, pages 110-117.
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Laura Roos, Hanne Jensen, Karen Grønskov, René Holst & Zeynep Tümer. (2016) Congenital Microphthalmia, Anophthalmia and Coloboma among Live Births in Denmark. Ophthalmic Epidemiology 23:5, pages 324-330.
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Mette Bertelsen, Hanne Jensen, Jesper F. Bregnhøj & Thomas Rosenberg. (2014) Prevalence of Generalized Retinal Dystrophy in Denmark. Ophthalmic Epidemiology 21:4, pages 217-223.
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Articles from other publishers (5)

Line Kessel, Jakob Kjellberg, Rikke Ibsen, Annette Rasmussen, Kamilla Rothe Nissen & Morten la Cour. (2022) Longitudinal analysis of health care costs in patients with childhood onset inherited retinal dystrophies compared to healthy controls. BMC Ophthalmology 22:1.
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Susan Silveira, Frank J. Martin, Maree Flaherty & Heather C. Russell. (2021) Reporting on Australian childhood visual impairment: the first 10 years. Eye 36:7, pages 1412-1418.
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Bart P. LeroyDavid G. BirchJacque L. DuncanByron L. LamRobert K. KoenekoopFernanda B. O. PortoStephen R. Russell & Aniz Girach. (2021) LEBER CONGENITAL AMAUROSIS DUE TO CEP290 MUTATIONS—SEVERE VISION IMPAIRMENT WITH A HIGH UNMET MEDICAL NEED. Retina 41:5, pages 898-907.
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Galuh D N Astuti, Mette Bertelsen, Markus N Preising, Muhammad Ajmal, Birgit Lorenz, Sultana M H Faradz, Raheel Qamar, Rob W J Collin, Thomas Rosenberg & Frans P M Cremers. (2015) Comprehensive genotyping reveals RPE65 as the most frequently mutated gene in Leber congenital amaurosis in Denmark. European Journal of Human Genetics 24:7, pages 1071-1079.
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Mette Bertelsen, Allan Linneberg & Thomas Rosenberg. (2015) Socio-economic characteristics of patients with generalized retinal dystrophy in Denmark. Acta Ophthalmologica 93:2, pages 134-140.
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