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Novel SCN5A Mutation in Amiodarone-responsive Multifocal Ventricular Ectopy-associated Cardiomyopathy
BACKGROUND: Mutations in SCN5A, encoding the cardiac sodium channel (Na(V)1.5) typically cause ventricular arrhythmia or conduction slowing. Recently, SCN5A mutations have been associated with heart failure combined with variable atrial and ventricular arrhythmia. Here we present the clinical, genet...
Αποθηκεύτηκε σε:
| Κύριοι συγγραφείς: | , , , , |
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| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
2014
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| Θέματα: | |
| Διαθέσιμο Online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4108519/ https://ncbi.nlm.nih.gov/pubmed/24815523 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.hrthm.2014.04.042 |
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