Targeted gene delivery by AAV

The potential utility for targeted gene addition has been recognized and a number of different approaches are currently under evaluation. A variety of viruses naturally establish latency by integrating their genome into the host genome. The non-pathogenic adeno-associated virus (AAV) is unique in it...

Ausführliche Beschreibung

Bibliographische Detailangaben

Veröffentlicht in:	Human gene therapy 2009-11, Vol.20 (11), p.1508-1508
Hauptverfasser:	Linden, M, Dutheil, N, Henckaerts, E
Format:	Artikel
Sprache:	eng
Schlagworte:	Adeno-associated virus
Online-Zugang:	Volltext
Tags:	Tag hinzufügen Keine Tags, Fügen Sie den ersten Tag hinzu!