Identification and Analysis of Genes Associated with Inherited Retinal Diseases
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Publisher
Springer New York
Link
http://link.springer.com/content/pdf/10.1007/978-1-4939-8669-9_1
Reference115 articles.
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2. Neveling K, den Hollander AI, Cremers FP, Collin RW (2013) Identification and analysis of inherited retinal disease genes. Methods Mol Biol 935:3–23. https://doi.org/10.1007/978-1-62703-080-9_1
3. Glockle N, Kohl S, Mohr J, Scheurenbrand T, Sprecher A, Weisschuh N, Bernd A, Rudolph G, Schubach M, Poloschek C, Zrenner E, Biskup S, Berger W, Wissinger B, Neidhardt J (2014) Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies. Eur J Hum Genet 22(1):99–104. https://doi.org/10.1038/ejhg.2013.72
4. den Hollander AI, Black A, Bennett J, Cremers FP (2010) Lighting a candle in the dark: advances in genetics and gene therapy of recessive retinal dystrophies. J Clin Invest 120(9):3042–3053. https://doi.org/10.1172/JCI42258
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