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Stem cell-based therapy for α(1)-antitrypsin deficiency
Human induced pluripotent stem cells offer the possibility of generating unlimited quantities of cells for autologous transplantation. By correcting the genetic defect underlying Z-allele α(1)-antitrypsin deficiency, we recently provided the first proof of principle for application of human induced...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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BioMed Central
2012
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3340548/ https://www.ncbi.nlm.nih.gov/pubmed/22340671 http://dx.doi.org/10.1186/scrt95 |