A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome
- DOI
- 10.1016/j.nbd.2016.12.009
- Published
- 2017-03
- Container
- Neurobiology of Disease
- Publisher
- Elsevier BV
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1016/j.nbd.2016.12.009,
title = {A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome},
author = {Valerie Matagne and Yann Ehinger and Lydia Saidi and Ana Borges-Correia and Martine Barkats and Marc Bartoli and Laurent Villard and Jean-Christophe Roux},
year = {2017},
journal = {Neurobiology of Disease},
doi = {10.1016/j.nbd.2016.12.009},
url = {https://doi.org/10.1016/j.nbd.2016.12.009}
}RIS
TY - JOUR TI - A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome AU - Valerie Matagne AU - Yann Ehinger AU - Lydia Saidi AU - Ana Borges-Correia AU - Martine Barkats AU - Marc Bartoli AU - Laurent Villard AU - Jean-Christophe Roux PY - 2017 JO - Neurobiology of Disease DO - 10.1016/j.nbd.2016.12.009 UR - https://doi.org/10.1016/j.nbd.2016.12.009 ER -
APA
Matagne, V., Ehinger, Y., Saidi, L., Borges-Correia, A., Barkats, M., Bartoli, M., Villard, L., & Roux, J. (2017). A codon-optimized Mecp2 transgene corrects breathing deficits and improves survival in a mouse model of Rett syndrome. Neurobiology of Disease. https://doi.org/10.1016/j.nbd.2016.12.009
Source records
- crossref · retrieved 2026-11-08T10:28:36.882Z