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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...
Autores principales: | Cao, Guangliang, Sun, Congli, Shen, Hualin, Qu, Dewei, Shen, Chuanlu, Lu, Haiqin |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
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 |
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