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MeCP2 in the regulation of neural activity: Rett syndrome pathophysiological perspectives
Rett syndrome (RTT), an X-linked neurodevelopment disorder, occurs in approximately one out of 10,000 females. Individuals afflicted by RTT display a constellation of signs and symptoms, affecting nearly every organ system. Most striking are the neurological manifestations, including regression of l...
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| Veröffentlicht in: | Degener Neurol Neuromuscul Dis |
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| Hauptverfasser: | , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Dove
2015
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7337177/ https://ncbi.nlm.nih.gov/pubmed/32669918 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.2147/DNND.S61269 |
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