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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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Detalles Bibliográficos
Main Authors: Taneja, Praveen, Ogier, Michael, Brooks-Harris, Gabriel, Schmid, Danielle A., Katz, David M., Nelson, Sacha B.
Formato: Artigo
Idioma:Inglês
Publicado: Society for Neuroscience 2009
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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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