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Serotonin Abnormalities in Dravet Syndrome Mice Before and After the Age of Seizure Onset
Dravet syndrome (DS) is a genetic form of severe epilepsy often associated with mutation of the SCN1A gene encoding the voltage gated sodium channel Nav1.1. Typically refractive to conventional therapy, serotonin neurotransmission may be an innovative target for treatment. To further understand the...
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| Pubblicato in: | Brain Res |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6922539/ https://ncbi.nlm.nih.gov/pubmed/31445030 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.brainres.2019.146399 |
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