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• W2078163685 abstract "Many mutations and deletions in the dystrophin gene, responsible for Duchenne muscular dystrophy (DMD), can be corrected at the posttranscriptional level by skipping specific exons. Here we show that long-term benefit can be obtained in the dystrophic mouse model through the use of adeno-associated viral vectors expressing antisense sequences: persistent exon skipping, dystrophin rescue, and functional benefit were observed 74 weeks after a single systemic administration. The therapeutic benefit was sufficient to preserve the muscle integrity of mice up to old age. These results indicate a possible long-term gene therapy treatment of the DMD pathology." @default.
• W2078163685 created "2016-06-24" @default.
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• W2078163685 date "2008-06-01" @default.
• W2078163685 modified "2023-10-14" @default.
• W2078163685 title "Long-Term Benefit of Adeno-Associated Virus/Antisense-Mediated Exon Skipping in Dystrophic Mice" @default.
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• W2078163685 doi "https://doi.org/10.1089/hum.2008.012" @default.
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