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Gene mutations in cardiac arrhythmias: a review of recent evidence in ion channelopathies
Over the past 15 years, molecular genetic studies have linked gene mutations to many inherited arrhythmogenic disorders, in particular, “ion channelopathies”, in which mutations in genes encode functional units of ion channels and/or their transporter-associated proteins in patients without primary...
| Autores principales: | , , , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Dove Medical Press
2013
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3699290/ https://www.ncbi.nlm.nih.gov/pubmed/23837003 http://dx.doi.org/10.2147/TACG.S29676 |