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Long-lasting beneficial effects of central serotonin receptor 7 stimulation in female mice modeling Rett syndrome
Rett syndrome (RTT) is a rare neurodevelopmental disorder, characterized by severe behavioral and physiological symptoms. Mutations in the methyl CpG binding protein 2 gene (MECP2) cause more than 95% of classic cases, and currently there is no cure for this devastating disorder. Recently we have de...
Αποθηκεύτηκε σε:
| Τόπος έκδοσης: | Front Behav Neurosci |
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| Κύριοι συγγραφείς: | , , , , , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
Frontiers Media S.A.
2015
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4396444/ https://ncbi.nlm.nih.gov/pubmed/25926782 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fnbeh.2015.00086 |
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