Gene therapy offers many conceptual advantages to treat muscle diseases, especially various forms of muscular dystrophies; however, it faces a number of unique challenges, including the need to deliver a therapeutic vector to all muscles throughout the body. In Muscle Gene Therapy: Methods and Prools, expert researchers in the field present a collection of techniques aimed at bridging the translational gap in muscle gene therapy between the prevalent rodent models and vitally important larger animal models. Divided into three sections, this volume examines basic prools for optimizing the muscle gene expression cassette and for evaluating the therapeutic outcomes, new developments in muscle gene therapy technology such as adeno—associated viral vector (AAV), oligonucleotide—mediated exon—skipping, and novel RNA—based strategies, and step—by—step guidance on muscle gene delivery in swine, ovine, canine, and non—human primates. Written in the highly successful Methods in Molecular Biology™ series format, chapters include introductions to their respective topics, lists of the necessary materials and reagents, detailed, readily reproducible laboratory prools, and tips on troubleshooting and avoiding known pitfalls. Authoritative and cutting—edge, Muscle Gene Therapy: Methods and Prools serves as an invaluable resource for graduate students, post—doctoral fellows, and principle investigators pursuing the crucial advancement of muscle disease gene therapy in the hope of someday curing these debilitating disorders.