A highly functional mini-dystrophin/GFP fusion gene for cell and gene therapy studies of Duchenne muscular dystrophy

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Human Molecular Genetics, Vol. 15, Iss. 10, 2006-05 ,pp. : 1610-1622

Oxford University Press

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Read-through compound 13 restores dystrophin expression and improves muscle function in the mdx mouse model for Duchenne muscular dystrophy

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Human Molecular Genetics, Vol. 21, Iss. 18, 2012-09 ,pp. : 4007-4020

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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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Human Molecular Genetics, Vol. 20, Iss. 2, 2011-01 ,pp. : 235-244

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Absence of α7 integrin in dystrophin-deficient mice causes a myopathy similar to Duchenne muscular dystrophy

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Screening 25 Dystrophin Gene Exons for Deletions in Arab Children with Duchenne Muscular Dystrophy

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