Author:
Chen Xue,Liu Xiaoxing,Sheng Xunlun,Gao Xiang,Zhang Xiumei,Li Zili,Li Huiping,Liu Yani,Rong Weining,Zhao Kanxing,Zhao Chen
Publisher
Springer Science and Business Media LLC
Reference30 articles.
1. Chen, X. et al. PRPF4 mutations cause autosomal dominant retinitis pigmentosa. Hum Mol Genet 23, 2926–2939 (2014).
2. Xu, L., Hu, L., Ma, K., Li, J. & Jonas, J. B. Prevalence of retinitis pigmentosa in urban and rural adult Chinese: The Beijing Eye Study. Eur J Ophthalmol 16, 865–866 (2006).
3. Dryja, T. P., Hahn, L. B., Kajiwara, K. & Berson, E. L. Dominant and digenic mutations in the peripherin/RDS and ROM1 genes in retinitis pigmentosa. Invest Ophthalmol Vis Sci 38, 1972–1982 (1997).
4. Kajiwara, K., Berson, E. L. & Dryja, T. P. Digenic retinitis pigmentosa due to mutations at the unlinked peripherin/RDS and ROM1 loci. Science 264, 1604–1608 (1994).
5. Buermans, H. P. & den Dunnen, J. T. Next generation sequencing technology: Advances and applications. Biochim Biophys Acta 1842, 1932–1941 (2014). 10.1016/j.bbadis.2014.06.015.
Cited by
26 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