Personalized Medicine in Cystic Fibrosis: Characterization of Eight Rare CFTR Variants in Intestinal Organoids and Cellular Models.
- DOI
- 10.1007/s40291-025-00806-5
- Published
- 2026 Jan
- Container
- Molecular diagnosis & therapy
- Publisher
- Not recorded
- Open access
- yes
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Cite this work
BibTeX
@article{allodium:10.1007/s40291-025-00806-5,
title = {Personalized Medicine in Cystic Fibrosis: Characterization of Eight Rare CFTR Variants in Intestinal Organoids and Cellular Models.},
author = {Railean V and Rodrigues CS and Pankonien I and Ramalho SS and Silva IAL and Doušová T and Castanhinha S and Azevedo P and Roda J and Farinha CM and Amaral MD},
year = {2026},
journal = {Molecular diagnosis \& therapy},
doi = {10.1007/s40291-025-00806-5},
url = {https://doi.org/10.1007/s40291-025-00806-5}
}RIS
TY - JOUR TI - Personalized Medicine in Cystic Fibrosis: Characterization of Eight Rare CFTR Variants in Intestinal Organoids and Cellular Models. AU - Railean V AU - Rodrigues CS AU - Pankonien I AU - Ramalho SS AU - Silva IAL AU - Doušová T AU - Castanhinha S AU - Azevedo P AU - Roda J AU - Farinha CM AU - Amaral MD PY - 2026 JO - Molecular diagnosis & therapy DO - 10.1007/s40291-025-00806-5 UR - https://doi.org/10.1007/s40291-025-00806-5 ER -
APA
V, R., CS, R., I, P., SS, R., IAL, S., T, D., S, C., P, A., J, R., CM, F., & MD, A. (2026). Personalized Medicine in Cystic Fibrosis: Characterization of Eight Rare CFTR Variants in Intestinal Organoids and Cellular Models.. Molecular diagnosis & therapy. https://doi.org/10.1007/s40291-025-00806-5
Source records
- pubmed · retrieved 2026-09-27T01:13:37.846Z