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Oxford University Press

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Paving the Way towards Antisense Therapy against Duchenne Muscular Dystrophy

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Dystrobrevin Deficiency at the Sarcolemma of Patients with Muscular Dystrophy

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Identification of transcripts from a subtraction library which might be responsible for the mild phenotype in an intrafamilially variable course of Duchenne muscular dystrophy

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Dystrophin conferral using human endothelium expressing HLA-E in the non-immunosuppressive murine model of Duchenne muscular dystrophy

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