Provided are antisense molecules capable of binding to a selected target site in the human dystrophin gene to induce exon skipping, and methods of use thereof to treat muscular dystrophy.本發明提供能夠結合人類肌縮蛋白(dystrophin)基因中之選定目標位點以誘導外顯子略過(exon skipping)之反義分子,及使用其治療肌肉萎縮症之方法。