Widespread long-term gene transfer to mouse skeletal muscles and heart.
Successful treatment of muscular disorders awaits an adapted gene delivery protocol. The clinically applicable technique used for hematopoietic cells which is centered around implantation of retrovirally modified cells may not prove sufficient for a reversal of phenotype when muscle diseases are con...
Gardado en:
| Publicado en: | J Clin Invest |
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| Principais autores: | , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
American Society for Clinical Investigation
1992
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC443142/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/1644927/ https://ncbi.nlm.nih.govhttps://doi.org/10.1172/JCI115902 |
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