FRRS1L gene replacement ameliorates disease phenotypes in the mouse model of developmental and epileptic encephalopathy 37
- DOI
- 10.1016/j.neurot.2026.e00961
- Published
- 2026-07
- Container
- Neurotherapeutics
- Publisher
- Elsevier BV
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.neurot.2026.e00961,
title = {FRRS1L gene replacement ameliorates disease phenotypes in the mouse model of developmental and epileptic encephalopathy 37},
author = {Mehrnaz Sheibani and Esther O. Alao and Ummay Mariam and Jun Wu and Sahba Kasiri and Afsaneh Talai and Jochen Schwenk and Bernd Fakler and Steven J. Gray and Berge A. Minassian},
year = {2026},
journal = {Neurotherapeutics},
doi = {10.1016/j.neurot.2026.e00961},
url = {https://doi.org/10.1016/j.neurot.2026.e00961}
}RIS
TY - JOUR TI - FRRS1L gene replacement ameliorates disease phenotypes in the mouse model of developmental and epileptic encephalopathy 37 AU - Mehrnaz Sheibani AU - Esther O. Alao AU - Ummay Mariam AU - Jun Wu AU - Sahba Kasiri AU - Afsaneh Talai AU - Jochen Schwenk AU - Bernd Fakler AU - Steven J. Gray AU - Berge A. Minassian PY - 2026 JO - Neurotherapeutics DO - 10.1016/j.neurot.2026.e00961 UR - https://doi.org/10.1016/j.neurot.2026.e00961 ER -
APA
Sheibani, M., Alao, E. O., Mariam, U., Wu, J., Kasiri, S., Talai, A., Schwenk, J., Fakler, B., Gray, S. J., & Minassian, B. A. (2026). FRRS1L gene replacement ameliorates disease phenotypes in the mouse model of developmental and epileptic encephalopathy 37. Neurotherapeutics. https://doi.org/10.1016/j.neurot.2026.e00961
Source records
- crossref · retrieved 2026-09-26T07:15:09.058Z