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Pathophysiology of Locus Ceruleus Neurons in a Mouse Model of Rett Syndrome
Rett syndrome (RTT) is a neurodevelopmental disorder caused by loss-of-function mutations in the Methyl-CpG-binding protein-2 (MECP2) gene and is characterized by derangements in cognition, behavior, motor control, respiration and autonomic homeostasis, as well as seizures. Deficits in norepinephrin...
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| Main Authors: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Society for Neuroscience
2009
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| Assuntos: | |
| Acceso en liña: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2846656/ https://ncbi.nlm.nih.gov/pubmed/19793977 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.3156-09.2009 |
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