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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 (IKs) channel. Arrhythmias in LQT1 are characterized by prolongation of the QT interval on ECG, as well...
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| Auteurs principaux: | , , |
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| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
Wiley
2016-10-01
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| Collection: | Journal of Arrhythmia |
| Sujets: | |
| Accès en ligne: | http://www.sciencedirect.com/science/article/pii/S1880427616000041 |
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