Genome Analysis for Inherited Retinal Disease: The State of the Art
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Publisher
Springer Singapore
Link
http://link.springer.com/content/pdf/10.1007/978-981-15-9184-6_12
Reference129 articles.
1. Liew G, Michaelides M, Bunce C. A comparison of the causes of blindness certifications in England and Wales in working age adults (16–64 years), 1999–2000 with 2009–2010. BMJ Open. 2014;4:e004015.
2. Buch H, Vinding T, La Cour M, Appleyard M, Jensen GB, Nielsen NV. Prevalence and causes of visual impairment and blindness among 9980 Scandinavian adults; the Copenhagen City eye study. Ophthalmology. 2004;111:53–61.
3. Al-Merjan JI, Pandova MG, Al-Ghanim M, Al-Wayel A, Al-Mutairi S. Ophthalmic epidemiology registered blindness and low vision in Kuwait. Ophthalmic Epidemiol. 2005;12(4):251–7.
4. Berger W, Kloeckener-Gruissem B, Neidhardt J. The molecular basis of human retinal and vitreoretinal diseases. Prog Retin Eye Res. 2010;29(5):335–75.
5. Hamel CP. Gene discovery and prevalence in inherited retinal dystrophies. C R Biol. 2014 Mar;337(3):160–6.
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1. Multidisciplinary team directed analysis of whole genome sequencing reveals pathogenic non-coding variants in molecularly undiagnosed inherited retinal dystrophies;Human Molecular Genetics;2022-09-09
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