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Recently, variable length dystrophin constructs have been characterized in models of Duchenne muscular dystrophy (DMD)

Here, Hichem Tasfaout & team describe a new method for using proteomics to evaluate the efficacy of three dystrophin-replacement approaches using AAV vectors.


1Department of Biochemistry, Molecular Biology and Biophysics, University of Minnesota — Twin Cities, Minneapolis, Minnesota, USA.

2Department of Neurology.

3Senator Paul D. Wellstone Muscular Dystrophy Specialized Research Center, and.

4Department of Biochemistry, University of Washington School of Medicine, Seattle, Washington, USA.

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