AAV hybrid serotypes: improved vectors for gene delivery.

Abstract

In recent years, significant efforts have been made on studying and engineering adeno-associated virus (AAV) capsid, in order to increase efficiency in targeting specific cell types that are non-permissive to wild type (wt) viruses and to improve efficacy in infecting only the cell type of interest. With our previous knowledge of the viral properties of the… (More)

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Cite this paper

@article{Choi2005AAVHS, title={AAV hybrid serotypes: improved vectors for gene delivery.}, author={Vivian W Choi and Douglas M Mccarty and Richard Jude Samulski}, journal={Current gene therapy}, year={2005}, volume={5 3}, pages={299-310} }