This detailed volume describes a spectrum of methods and prools that can be used for the bench-to-bedside development and evaluation of retinal gene therapy. Methods for the successful delivery of these gene therapy vector systems to the retina are examined, as well as assays to test the efficacy in vitro in cell cultures, for gene augmentation and gene editing in vivo on rodents, pigs, and monkey retinas, and on human retinal explants as well as in human clinical studies. Written for the highly successful series, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible prools, and tips on troubleshooting and avoiding known pitfalls. Authoritative and practical, provides a wide range of readers from students to research experts with vital information on ocular gene therapy vector technology, and biological assays, and clinical prools, to promote further studies for the benefit of children and adults with inherited retinal disease.