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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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| Publicat a: | Front Neurol |
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| Autors principals: | , , , , , , , , , , , |
| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Frontiers Media S.A.
2020
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| Matèries: | |
| Accés en línia: | 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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