Lentiviral vector mediated gene transfer to the liver: transcriptional targeting of heterologous genes depends upon choice of both promoter and enhancer

Authors

Kathryn L. Nash, University of Cambridge
Bushra Jamil, Aga Khan UniversityFollow
Graeme J Alexander, University of Cambridge
Andrew M. Lever, University of Cambridge

Document Type

Article

Department

Medicine

Publication (Name of Journal)

Molecular Therapy

Recommended Citation

Nash, K., Jamil, B., Alexander, G., Lever, A. (2003). Lentiviral vector mediated gene transfer to the liver: transcriptional targeting of heterologous genes depends upon choice of both promoter and enhancer. Molecular Therapy, 7(5), S339.
Available at: https://ecommons.aku.edu/pakistan_fhs_mc_med_med/486