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Correlations in timing of sodium channel expression, epilepsy, and sudden death in Dravet syndrome
Dravet Syndrome (DS) is an intractable genetic epilepsy caused by loss‐of‐function mutations in SCN1A, the gene encoding brain sodium channel Na(v)1.1. DS is associated with increased frequency of sudden unexpected death in humans and in a mouse genetic model of this disease. Here we correlate the t...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Landes Bioscience
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4042481/ https://ncbi.nlm.nih.gov/pubmed/23965409 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4161/chan.26023 |
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