Association of NR2E3 but Not NRL Mutations with Retinitis Pigmentosa in the Chinese Population
Publication in refereed journal


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摘要PURPOSE. Mutations in the NR2E3 and NRL genes have been implicated in both autosomal dominant and autosomal recessive retinitis pigmentosa (RP). In this study, the mutation profiles of these two genes were investigated in Chinese RP patients.
著者Yang YP, Zhang X, Chen LJ, Chiang SWY, Tam POS, Lai TYY, Chan CKM, Wang NL, Lam DSC, Pang CP
期刊名稱Investigative Ophthalmology & Visual Science
出版年份2010
月份4
日期1
卷號51
期次4
出版社Association for Research in Vision and Ophthalmology (ARVO)
頁次2229 - 2235
國際標準期刊號0146-0404
電子國際標準期刊號1552-5783
語言英式英語
Web of Science 學科類別Ophthalmology; OPHTHALMOLOGY

上次更新時間 2021-05-04 於 23:52