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Insights into the molecular mechanisms of bradycardia-triggered arrhythmias in long QT-3 syndrome
Congenital long QT syndrome is a rare disease in which the electrocardiogram QT interval is prolonged due to dysfunctional ventricular repolarization. Variant 3 (LQT-3) is associated with mutations in SCN5A, the gene coding for the heart Na(+) channel α subunit. Arrhythmias in LQT-3 mutation carrier...
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| Asıl Yazarlar: | , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
American Society for Clinical Investigation
2002
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC151612/ https://ncbi.nlm.nih.gov/pubmed/12417563 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI15928 |
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