首页 | 本学科首页   官方微博 | 高级检索  
     


Retinal AAV8-RS1 Gene Therapy for X-Linked Retinoschisis: Initial Findings from a Phase I/IIa Trial by Intravitreal Delivery
Authors:Catherine Cukras  Henry E. Wiley  Brett G. Jeffrey  H. Nida Sen  Amy Turriff  Yong Zeng  Camasamudram Vijayasarathy  Dario Marangoni  Lucia Ziccardi  Sten Kjellstrom  Tae Kwon Park  Suja Hiriyanna  J. Fraser Wright  Peter Colosi  Zhijian Wu  Ronald A. Bush  Lisa L. Wei  Paul A. Sieving
Affiliation:1. NIH, National Eye Institute, Bethesda, MD 20892, USA;2. STRRMD/NIDCD/NIH, Bethesda, MD 20874, USA;3. Neurophysiology of Vision and Neuropathmology Unit, IRCCS Fondazione G.B. Bietti, Rome 00198, Italy;4. Department of Ophthalmology, Lund University, Lund, Sweden;5. Ophthalomology, Soonchunhyang University Bucheon Hospital, Seoul, Korea;6. Ocular Gene Therapy Core, National Eye Institute, Bethesda, MD 20892, USA;7. Ophthalomology, Children’s Hospital of Philadelphia, Philadelphia, PA, USA
Abstract:
Keywords:gene therapy  X-linked retinoschisis  clinical trial  AAV vector  ocular disease  retinal disease
本文献已被 ScienceDirect 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号