Retroviral vectors for gene therapy of Duchenne muscular dystrophy

Abstract

The aim of this review is to summarize the state of art of retroviral vectors for gene therapy of Duchenne muscular dystrophy (DMD). Acutal knowledge on this matter indicates that retroviral vectors are able to transduce muscle satellite cells in vivo and that these cells can participate in muscle repair processes, even if the efficiency of transduction of… (More)
DOI: 10.1007/s100720070005

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Cite this paper

@article{Fassati2000RetroviralVF, title={Retroviral vectors for gene therapy of Duchenne muscular dystrophy}, author={Ariberto Fassati and Nereo Bresolin}, journal={Neurological Sciences}, year={2000}, volume={21}, pages={S925-S927} }