Scholars@Duke publication: A Novel Human Liver Chimeric Mouse Model Lacking the Murine <i>AAVR</i> Gene for Validation of AAV Gene Therapy Vectors

A Novel Human Liver Chimeric Mouse Model Lacking the Murine AAVR Gene for Validation of AAV Gene Therapy Vectors

Publication , Conference

Chen, T; Barzi, M; Pankowicz, F; Gonzalez, TJ; Bissig-Choisat, B; Asokan, A; Bissig, K-D

Published in: MOLECULAR THERAPY

2022

MOLECULAR THERAPY

1525-0024

1525-0016

2022

43 / 43

APA

Chicago

ICMJE

MLA

NLM

Chen, T., Barzi, M., Pankowicz, F., Gonzalez, T. J., Bissig-Choisat, B., Asokan, A., & Bissig, K.-D. (2022). A Novel Human Liver Chimeric Mouse Model Lacking the Murine AAVR Gene for Validation of AAV Gene Therapy Vectors. In MOLECULAR THERAPY (Vol. 30, pp. 43–43).

Chen, Tong, Mercedes Barzi, Francis Pankowicz, Trevor J. Gonzalez, Beatrice Bissig-Choisat, Aravind Asokan, and Karl-Dimiter Bissig. “A Novel Human Liver Chimeric Mouse Model Lacking the Murine AAVR Gene for Validation of AAV Gene Therapy Vectors.” In MOLECULAR THERAPY, 30:43–43, 2022.

Chen T, Barzi M, Pankowicz F, Gonzalez TJ, Bissig-Choisat B, Asokan A, et al. A Novel Human Liver Chimeric Mouse Model Lacking the Murine AAVR Gene for Validation of AAV Gene Therapy Vectors. In: MOLECULAR THERAPY. 2022. p. 43–43.

Chen T, Barzi M, Pankowicz F, Gonzalez TJ, Bissig-Choisat B, Asokan A, Bissig K-D. A Novel Human Liver Chimeric Mouse Model Lacking the Murine AAVR Gene for Validation of AAV Gene Therapy Vectors. MOLECULAR THERAPY. 2022. p. 43–43.

MOLECULAR THERAPY

1525-0024

1525-0016

2022

43 / 43