Functional Network Mapping Reveals State-Dependent Response to IGF1 Treatment in Rett Syndrome

Rett Syndrome (RTT) is a neurodevelopmental disorder associated with mutations in the gene MeCP2, which is involved in the development and function of cortical networks. The clinical presentation of RTT is generally severe and includes developmental regression and marked neurologic impairment. Insul...

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Detalles Bibliográficos
Autores principales: Keogh, Conor, Pini, Giorgio, Gemo, Ilaria, Kaufmann, Walter E., Tropea, Daniela
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465931/
https://www.ncbi.nlm.nih.gov/pubmed/32756423
http://dx.doi.org/10.3390/brainsci10080515

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7465931/
https://www.ncbi.nlm.nih.gov/pubmed/32756423
http://dx.doi.org/10.3390/brainsci10080515

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