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Query Trace: Retinal Diseases and PRPH2[original query]

Exome Sequencing on 298 Probands With Early-Onset High Myopia: Approximately One-Fourth Show Potential Pathogenic Mutations in RetNet Genes. Investigative ophthalmology & visual science 2015 Dec 56 (13): 8365-72. Sun Wenmin, Huang Li, Xu Yan, Xiao Xueshan, Li Shiqiang, Jia Xiaoyun, Gao Bei, Wang Panfeng, Guo Xiangming, Zhang Qingjio Similar articles in PubMed
Comprehensive molecular diagnosis of 179 Leber congenital amaurosis and juvenile retinitis pigmentosa patients by targeted next generation sequencing. Journal of medical genetics 2013 Oct 50 (10): 674-88. Wang Xia, Wang Hui, Sun Vincent, Tuan Han-Fang, Keser Vafa, Wang Keqing, Ren Huanan, Lopez Irma, Zaneveld Jacques E, Siddiqui Sorath, Bowles Stephanie, Khan Ayesha, Salvo Jason, Jacobson Samuel G, Iannaccone Alessandro, Wang Feng, Birch David, Heckenlively John R, Fishman Gerald A, Traboulsi Elias I, Li Yumei, Wheaton Dianna, Koenekoop Robert K, Chen R Similar articles in PubMed