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Cardiac sodium channelopathy associated with SCN5A mutations: electrophysiological, molecular and genetic aspects
Over the last two decades, an increasing number of SCN5A mutations have been described in patients with long QT syndrome type 3 (LQT3), Brugada syndrome, (progressive) conduction disease, sick sinus syndrome, atrial standstill, atrial fibrillation, dilated cardiomyopathy, and sudden infant death syn...
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Blackwell Science Inc
2013
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3779105/ https://ncbi.nlm.nih.gov/pubmed/23818691 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1113/jphysiol.2013.256461 |
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