Upregulation of RBFOX1 in the malformed cortex of patients with intractable epilepsy and in cultured rat neurons

Mutations in RNA-binding Fox 1 (RBFOX1) are known to be associated with neurodevelopmental disorders including epilepsy, mental retardation and autism spectrum disorder. The deletion of the Rbfox1 gene in mice has been shown to result in heightened susceptibility to seizures. However, other studies...

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Detalles Bibliográficos
Autores principales: WEN, MING, YAN, YONG, YAN, NING, CHEN, XIAO SHAN, LIU, SHI YONG, FENG, ZHAN HUI
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2015
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314424/
https://www.ncbi.nlm.nih.gov/pubmed/25571999
http://dx.doi.org/10.3892/ijmm.2015.2061

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4314424/
https://www.ncbi.nlm.nih.gov/pubmed/25571999
http://dx.doi.org/10.3892/ijmm.2015.2061

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