Author:
Haer-Wigman Lonneke,van Zelst-Stams Wendy AG,Pfundt Rolph,van den Born L Ingeborgh,Klaver Caroline CW,Verheij Joke BGM,Hoyng Carel B,Breuning Martijn H,Boon Camiel JF,Kievit Anneke J,Verhoeven Virginie JM,Pott Jan WR,Sallevelt Suzanne CEH,van Hagen Johanna M,Plomp Astrid S,Kroes Hester Y,Lelieveld Stefan H,Hehir-Kwa Jayne Y,Castelein Steven,Nelen Marcel,Scheffer Hans,Lugtenberg Dorien,Cremers Frans PM,Hoefsloot Lies,Yntema Helger G
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference25 articles.
1. Kocur I, Resnikoff S : Visual impairment and blindness in Europe and their prevention. Br J Ophthalmol 2002; 86: 716–722.
2. Finger RP, Fimmers R, Holz FG, Scholl HP : Incidence of blindness and severe visual impairment in Germany: projections for 2030. Invest Ophthalmol Vis Sci 2011; 52: 4381–4389.
3. Ayuso C, Millan JM : Retinitis pigmentosa and allied conditions today: a paradigm of translational research. Genome Med 2010; 2: 34.
4. Sahel JA, Marazova K, Audo I : Clinical characteristics and current therapies for inherited retinal degenerations. Cold Spring Harb Perspect Med 2015; 5: a017111.
5. Rahi JS, Dezateux C,, British Congenital Cataract Interest G: Measuring and interpreting the incidence of congenital ocular anomalies: lessons from a national study of congenital cataract in the UK. Invest Ophthalmol Vis Sci 2001; 42: 1444–1448.
Cited by
108 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献