Conditional Deletion of Foxg1 Delayed Myelination during Early Postnatal Brain Development

FOXG1 (forkhead box G1) syndrome is a neurodevelopmental disorder caused by variants in the Foxg1 gene that affect brain structure and function. Individuals affected by FOXG1 syndrome frequently exhibit delayed myelination in neuroimaging studies, which may impair the rapid conduction of nerve impul...

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Detalles Bibliográficos
Autores principales: Cao, Guangliang, Sun, Congli, Shen, Hualin, Qu, Dewei, Shen, Chuanlu, Lu, Haiqin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10530892/
https://www.ncbi.nlm.nih.gov/pubmed/37762220
http://dx.doi.org/10.3390/ijms241813921

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10530892/
https://www.ncbi.nlm.nih.gov/pubmed/37762220
http://dx.doi.org/10.3390/ijms241813921

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