Behavioral and brain anatomical analysis of Foxg1 heterozygous mice

FOXG1 Syndrome (FS) is a devastating neurodevelopmental disorder that is caused by a heterozygous loss-of-function (LOF) mutation of the FOXG1 gene, which encodes a transcriptional regulator important for telencephalic brain development. People with FS have marked developmental delays, impaired ambu...

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Detalles Bibliográficos
Autores principales: Erickson, Kirsty R., Farmer, Rebekah, Merritt, Jonathan K., Miletic Lanaghan, Zeljka, Does, Mark D., Ramadass, Karthik, Landman, Bennett A., Cutting, Laurie E., Neul, Jeffrey L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2022
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555627/
https://www.ncbi.nlm.nih.gov/pubmed/36223387
http://dx.doi.org/10.1371/journal.pone.0266861

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9555627/
https://www.ncbi.nlm.nih.gov/pubmed/36223387
http://dx.doi.org/10.1371/journal.pone.0266861

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