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A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation
BACKGROUND: Mutations in the SCN5A gene, encoding the α-subunit of the cardiac Na(+) channel, Na(v)1.5, can result in several life-threatening arrhythmias. OBJECTIVE: To characterize a distal truncating SCN5A mutation, R1860Gfs*12, identified in a family with different phenotypes including sick sinu...
Tallennettuna:
| Päätekijät: | , , , , , , , , , , |
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| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2014
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4056672/ https://ncbi.nlm.nih.gov/pubmed/24582607 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.hrthm.2014.02.021 |
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