Behavioral Phenotypes of Foxg1 Heterozygous Mice

FOXG1 syndrome (FS, aka a congenital variant of Rett syndrome) is a recently defined rare and devastating neurodevelopmental disorder characterized by various symptoms, including severe intellectual disability, autistic features, involuntary, and continuous jerky movements, feeding problems, sleep d...

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Detalles Bibliográficos
Autores principales: Younger, Skyler, Boutros, Sydney, Cargnin, Francesca, Jeon, Shin, Lee, Jae W., Lee, Soo-Kyung, Raber, Jacob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Pharmacology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214218/
https://www.ncbi.nlm.nih.gov/pubmed/35754477
http://dx.doi.org/10.3389/fphar.2022.927296

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9214218/
https://www.ncbi.nlm.nih.gov/pubmed/35754477
http://dx.doi.org/10.3389/fphar.2022.927296

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