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Genetic correction of dystrophin deficiency and skeletal muscle remodeling in adult MDX mouse via transplantation of retroviral producer cells.

Duchenne muscular dystrophy (DMD) is an X-linked, lethal disease caused by mutations of the dystrophin gene. No effective therapy is available, but dystrophin gene transfer to skeletal muscle has been proposed as a treatment for DMD. We have developed a strategy for efficient in vivo gene transfer o...

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Detalhes bibliográficos
Main Authors: Fassati, A, Wells, D J, Sgro Serpente, P A, Walsh, F S, Brown, S C, Strong, P N, Dickson, G
Formato: Artigo
Idioma:Inglês
Publicado em: 1997
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Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC508230/
https://ncbi.nlm.nih.gov/pubmed/9239410
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