Abstract: Sequences of novel adeno-associated virus capsids and vectors and host cells containing these sequences are provided. Also described are methods of using such host cells and vectors in production of rAAV particles. AAV-mediated delivery of therapeutic and immunogenic genes using the vectors of the invention is also provided.
September 30, 2004
February 15, 2007
The Trutees of the University of Pennsylvania
James Wilson, Guangping Gao, Mauricio Alvira, Luc Vandenberghe