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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Detalhes bibliográficos
Publicado no:Front Neurol
Main Authors: 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: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2020
Assuntos:
Neurology
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7662121/
https://ncbi.nlm.nih.gov/pubmed/33193060
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2020.593554
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