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Evading the immune response upon in vivo gene therapy with viral vectors

Gene therapy has the potential to provide minimally invasive and long-term treatment for many inherited disorders that otherwise have poor prognoses and limited treatment options. The sustained therapeutic correction of genetic disease by viral gene transfer has been accomplished in patients with se...

Ausführliche Beschreibung

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Bibliographische Detailangaben
Hauptverfasser: Sack, Brandon K, Herzog, Roland W
Format: Artigo
Sprache:Inglês
Veröffentlicht: 2009
Schlagworte:
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC3584155/
https://ncbi.nlm.nih.gov/pubmed/19806497
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