Retinitis Pigmentosa in Japanese Population
Author:
Publisher
Springer Japan
Link
http://link.springer.com/content/pdf/10.1007/978-4-431-56511-6_11
Reference67 articles.
1. Abd El-Aziz MM, Barragan I, O’Driscoll CA, et al. EYS, encoding an ortholog of Drosophila spacemaker, is mutated in autosomal recessive retinitis pigmentosa. Nat Genet. 2008;40(11):1285–7.
2. Abd El-Aziz MM, O’Driscoll CA, Kaye RS, et al. Identification of novel mutations in the ortholog of Drosophila eyes shut gene (EYS) causing autosomal recessive retinitis pigmentosa. Invest Ophthalmol Vis Sci. 2010;51(8):4266–72.
3. Aller E, Jaijo T, Beneyto M, et al. Identification of 14 novel mutations in the long isoform of USH2A in Spanish patients with Usher syndrome type II. J Med Genet. 2006;43(11):e55.
4. Arai Y, Maeda A, Hirami Y, et al. Retinitis pigmentosa with EYS mutations is the most prevalent inherited retinal dystrophy in Japanese populations. J Ophthalmol. 2015;2015:819760.
5. Audo I, Sahel JA, Mohand-Said S, et al. EYS is a major gene for rod-cone dystrophies in France. Hum Mutat. 2010;31(5):E1406–35.
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