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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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Detalhes bibliográficos
Publicado no:Brain Res
Main Authors: Hatini, Paul G., Commons, Kathryn G.
Formato: Artigo
Idioma:Inglês
Publicado em: 2019
Assuntos:
Acesso em linha: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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