Title: Identification of two novel mutations (E332X and c1536delC) in the RPGR gene in two Chinese families with X-linked retinitis pigmentosa
Abstract: Human MutationVolume 15, Issue 6 p. 584-584 Mutation and Polymorphism Report Identification of two novel mutations (E332X and c1536delC) in the RPGR gene in two Chinese families with X-linked retinitis pigmentosa † Li Liu, Li Liu Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this authorLei Jin, Lei Jin Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this authorMugen Liu, Mugen Liu Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this authorYong Wei, Yong Wei Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this authorXuejun Wu, Xuejun Wu Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this authorYe Liu, Ye Liu Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this authorYoue Liu, Youe Liu Ophthalmic Hospital of Zhabei District, Shanghai, ChinaSearch for more papers by this authorHonghai Wang, Honghai Wang Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this authorRenyuan Chu, Renyuan Chu Affiliated Ophthalmic Hospital of Shanghai Medical University, Shanghai, ChinaSearch for more papers by this authorJianhua Chai, Jianhua Chai Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this author Li Liu, Li Liu Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this authorLei Jin, Lei Jin Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this authorMugen Liu, Mugen Liu Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this authorYong Wei, Yong Wei Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this authorXuejun Wu, Xuejun Wu Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this authorYe Liu, Ye Liu Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this authorYoue Liu, Youe Liu Ophthalmic Hospital of Zhabei District, Shanghai, ChinaSearch for more papers by this authorHonghai Wang, Honghai Wang Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this authorRenyuan Chu, Renyuan Chu Affiliated Ophthalmic Hospital of Shanghai Medical University, Shanghai, ChinaSearch for more papers by this authorJianhua Chai, Jianhua Chai Institute of Genetics, Fudan University, Shanghai, ChinaSearch for more papers by this author First published: 31 May 2000 https://doi.org/10.1002/1098-1004(200006)15:6<584::AID-HUMU26>3.0.CO;2-OCitations: 6 † Communicated by: Daniel F. Schorderet ‡ Online Citation: Human Mutation, Mutation and Polymorphism Report #127 (2000) Online http://journals.wiley.com/1059-7794/pdf/mutation/mpr127.pdf § Acknowledgments: The authors thank both families for their contributions to the study and Mr. Yipeng Wang for helping in obtaining blood samples. The study is supported by High Technology Developmental Program and National Natural Science Foundation of China. AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article.Citing Literature Volume15, Issue6June 2000Pages 584-584 RelatedInformation