Novel AAV843 Vector-Mediated Gene Replacement Therapy Rescues Primary Hyperoxaluria Type I in Mice.
- DOI
- 10.3390/cells15070629
- Published
- 2026 Mar 31
- Container
- Cells
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.3390/cells15070629,
title = {Novel AAV843 Vector-Mediated Gene Replacement Therapy Rescues Primary Hyperoxaluria Type I in Mice.},
author = {Zhang J and Yin Y and Ji B and Sun M and Jiang Y and Wu X and Xiao X and Shen Q and Wu X and Xu H},
year = {2026},
journal = {Cells},
doi = {10.3390/cells15070629},
url = {https://doi.org/10.3390/cells15070629}
}RIS
TY - JOUR TI - Novel AAV843 Vector-Mediated Gene Replacement Therapy Rescues Primary Hyperoxaluria Type I in Mice. AU - Zhang J AU - Yin Y AU - Ji B AU - Sun M AU - Jiang Y AU - Wu X AU - Xiao X AU - Shen Q AU - Wu X AU - Xu H PY - 2026 JO - Cells DO - 10.3390/cells15070629 UR - https://doi.org/10.3390/cells15070629 ER -
APA
J, Z., Y, Y., B, J., M, S., Y, J., X, W., X, X., Q, S., X, W., & H, X. (2026). Novel AAV843 Vector-Mediated Gene Replacement Therapy Rescues Primary Hyperoxaluria Type I in Mice.. Cells. https://doi.org/10.3390/cells15070629
Source records
- pubmed · retrieved 2026-09-27T00:38:38.315Z