Loss of MeCP2 Function Across Several Neuronal Populations Impairs Breathing Response to Acute Hypoxia

Rett Syndrome (RTT) is a neurodevelopmental disorder caused by loss of function of the transcriptional regulator Methyl-CpG-Binding Protein 2 (MeCP2). In addition to the characteristic loss of hand function and spoken language after the first year of life, people with RTT also have a variety of phys...

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Detalles Bibliográficos
Autores principales: Ward, Christopher S., Huang, Teng-Wei, Herrera, Jose A., Samaco, Rodney C., McGraw, Christopher M., Parra, Diana E., Arvide, E. Melissa, Ito-Ishida, Aya, Meng, Xiangling, Ure, Kerstin, Zoghbi, Huda Y., Neul, Jeffrey L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Neurology
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662121/
https://www.ncbi.nlm.nih.gov/pubmed/33193060
http://dx.doi.org/10.3389/fneur.2020.593554

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7662121/
https://www.ncbi.nlm.nih.gov/pubmed/33193060
http://dx.doi.org/10.3389/fneur.2020.593554

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