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Molecular pathogenesis of long QT syndrome type 1
Long QT syndrome type 1 (LQT1) is a subtype of a congenital cardiac syndrome caused by mutation in the KCNQ1 gene, which encodes the α-subunit of the slow component of delayed rectifier K(+) current (I(Ks)) channel. Arrhythmias in LQT1 are characterized by prolongation of the QT interval on ECG, as...
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| Publicado en: | J Arrhythm |
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| Autores principales: | , , |
| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
Elsevier
2016
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5063268/ https://ncbi.nlm.nih.gov/pubmed/27761162 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.joa.2015.12.006 |
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