Pharmacological readthrough and base editing for ANK1 nonsense mutations in an erythroid model of hereditary spherocytosis.
- DOI
- 10.1016/j.omtn.2026.103053
- Published
- 2026 Sep 8
- Container
- Molecular therapy. Nucleic acids
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1016/j.omtn.2026.103053,
title = {Pharmacological readthrough and base editing for ANK1 nonsense mutations in an erythroid model of hereditary spherocytosis.},
author = {Li S and Li J and Shi W and Nie Z and Zhang S and Ding X and Hu J and Li P and Xie X},
year = {2026},
journal = {Molecular therapy. Nucleic acids},
doi = {10.1016/j.omtn.2026.103053},
url = {https://doi.org/10.1016/j.omtn.2026.103053}
}RIS
TY - JOUR TI - Pharmacological readthrough and base editing for ANK1 nonsense mutations in an erythroid model of hereditary spherocytosis. AU - Li S AU - Li J AU - Shi W AU - Nie Z AU - Zhang S AU - Ding X AU - Hu J AU - Li P AU - Xie X PY - 2026 JO - Molecular therapy. Nucleic acids DO - 10.1016/j.omtn.2026.103053 UR - https://doi.org/10.1016/j.omtn.2026.103053 ER -
APA
S, L., J, L., W, S., Z, N., S, Z., X, D., J, H., P, L., & X, X. (2026). Pharmacological readthrough and base editing for ANK1 nonsense mutations in an erythroid model of hereditary spherocytosis.. Molecular therapy. Nucleic acids. https://doi.org/10.1016/j.omtn.2026.103053
Source records
- pubmed · retrieved 2026-09-25T22:23:58.019Z