MeCP2 Deficiency Leads to Loss of Glial Kir4.1

Rett syndrome (RTT) is an X-linked neurodevelopmental disorder usually caused by mutations in methyl-CpG-binding protein 2 (MeCP2). RTT is typified by apparently normal development until 6–18 mo of age, when motor and communicative skills regress and hand stereotypies, autonomic symptoms, and seizur...

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Detalles Bibliográficos
Autores principales: Kahanovitch, Uri, Cuddapah, Vishnu A., Pacheco, Natasha L., Holt, Leanne M., Mulkey, Daniel K., Percy, Alan K., Olsen, Michelle L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Society for Neuroscience 2018
Materias:
New Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818552/
https://www.ncbi.nlm.nih.gov/pubmed/29464197
http://dx.doi.org/10.1523/ENEURO.0194-17.2018

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5818552/
https://www.ncbi.nlm.nih.gov/pubmed/29464197
http://dx.doi.org/10.1523/ENEURO.0194-17.2018

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