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Early-life febrile seizures worsen adult phenotypes in Scn1a mutants
Mutations in the voltage-gated sodium channel (VGSC) gene SCN1A, encoding the Na(v)1.1 channel, are responsible for a number of epilepsy disorders including genetic epilepsy with febrile seizures plus (GEFS+) and Dravet syndrome (DS). Patients with SCN1A mutations often experience prolonged early-li...
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| Publicado no: | Exp Neurol |
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| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2017
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5538963/ https://ncbi.nlm.nih.gov/pubmed/28373025 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.expneurol.2017.03.026 |
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