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- W2014119697 abstract "Although 20 years have elapsed since scientists identified the protein encoded by the defective gene that causes Duchenne muscular dystrophy (DMD), treatment options to help slow the disease's progressive muscle degeneration have remained limited." @default.
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- W2014119697 title "Studies Point Way to New Therapeutic Prospects for Muscular Dystrophy" @default.
- W2014119697 doi "https://doi.org/10.1001/jama.298.12.1385" @default.
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