Author:
Glöckle Nicola,Kohl Susanne,Mohr Julia,Scheurenbrand Tim,Sprecher Andrea,Weisschuh Nicole,Bernd Antje,Rudolph Günther,Schubach Max,Poloschek Charlotte,Zrenner Eberhart,Biskup Saskia,Berger Wolfgang,Wissinger Bernd,Neidhardt John
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference28 articles.
1. Berger W, Kloeckener-Gruissem B, Neidhardt J : The molecular basis of human retinal and vitreoretinal diseases. Prog Retin Eye Res 2010; 29: 335–375.
2. Hartong DT, Berson EL, Dryja TP : Retinitis pigmentosa. Lancet 2006; 368: 1795–1809.
3. Avila-Fernandez A, Cantalapiedra D, Aller E et al: Mutation analysis of 272 Spanish families affected by autosomal recessive retinitis pigmentosa using a genotyping microarray. Mol Vis 2010; 16: 2550–2558.
4. Zeitz C, Labs S, Lorenz B et al: Genotyping microarray for CSNB-associated genes. Invest Ophthalmol Vis Sci 2009; 50: 5919–5926.
5. Zernant J, Kulm M, Dharmaraj S et al: Genotyping microarray (disease chip) for Leber congenital amaurosis: detection of modifier alleles. Invest Ophthalmol Vis Sci 2005; 46: 3052–3059.
Cited by
212 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