Modeling Mowat-Wilson syndrome with patient iPSCs reveals transcriptional and phenotypic defects in neural progenitors.
- DOI
- 10.1016/j.nbd.2025.107205
- Published
- 2026 Jan
- Container
- Neurobiology of disease
- Publisher
- Not recorded
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.nbd.2025.107205,
title = {Modeling Mowat-Wilson syndrome with patient iPSCs reveals transcriptional and phenotypic defects in neural progenitors.},
author = {Musante I and Gorrieri G and Tamburro S and Ferrera G and Baldassari S and Fetta A and Caraffi SG and Vignoli A and Fiorito G and Garavelli L and Canevini MP and Cordelli DM and Zara F and Ricci E and Scudieri P},
year = {2026},
journal = {Neurobiology of disease},
doi = {10.1016/j.nbd.2025.107205},
url = {https://doi.org/10.1016/j.nbd.2025.107205}
}RIS
TY - JOUR TI - Modeling Mowat-Wilson syndrome with patient iPSCs reveals transcriptional and phenotypic defects in neural progenitors. AU - Musante I AU - Gorrieri G AU - Tamburro S AU - Ferrera G AU - Baldassari S AU - Fetta A AU - Caraffi SG AU - Vignoli A AU - Fiorito G AU - Garavelli L AU - Canevini MP AU - Cordelli DM AU - Zara F AU - Ricci E AU - Scudieri P PY - 2026 JO - Neurobiology of disease DO - 10.1016/j.nbd.2025.107205 UR - https://doi.org/10.1016/j.nbd.2025.107205 ER -
APA
I, M., G, G., S, T., G, F., S, B., A, F., SG, C., A, V., G, F., L, G., MP, C., DM, C., F, Z., E, R., & P, S. (2026). Modeling Mowat-Wilson syndrome with patient iPSCs reveals transcriptional and phenotypic defects in neural progenitors.. Neurobiology of disease. https://doi.org/10.1016/j.nbd.2025.107205
Source records
- pubmed · retrieved 2026-09-27T07:01:02.447Z