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Plos One|February 17, 2016
AAV-Mediated Clarin-1 Expression in the Mouse Retina: Implications for USH3A Gene TherapyAstra Dinculescu, Rachel M Stupay, Wen-Tao Deng, et al.Human Gene Therapy|December 6, 2012
AAV-mediated gene therapy in the guanylate cyclase (RetGC1/RetGC2) double knockout mouse model of Leber congenital amaurosisSanford L Boye, Igor V Peshenko, Wei Chieh Huang, et al.Molecular Therapy. Methods & Clinical Development|April 25, 2014
Targeted CNS Delivery Using Human MiniPromoters and Demonstrated Compatibility with Adeno-Associated Viral VectorsCharles N de Leeuw, Frank M Dyka, Sanford L Boye, et al.Pageof 3