Glial Dysfunction in MeCP2 Deficiency Models: Implications for Rett Syndrome

Rett syndrome (RTT) is a rare, X-linked neurodevelopmental disorder typically affecting females, resulting in a range of symptoms including autistic features, intellectual impairment, motor deterioration, and autonomic abnormalities. RTT is primarily caused by the genetic mutation of the Mecp2 gene....

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Detalles Bibliográficos
Autores principales: Kahanovitch, Uri, Patterson, Kelsey C., Hernandez, Raymundo, Olsen, Michelle L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6696322/
https://www.ncbi.nlm.nih.gov/pubmed/31387202
http://dx.doi.org/10.3390/ijms20153813

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6696322/
https://www.ncbi.nlm.nih.gov/pubmed/31387202
http://dx.doi.org/10.3390/ijms20153813

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