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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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Detalles Bibliográficos
Autores principales:	Wu, Jie, Ding, Wei-Guang, Horie, Minoru
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2016
Materias:	Review
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5063268/ https://www.ncbi.nlm.nih.gov/pubmed/27761162 http://dx.doi.org/10.1016/j.joa.2015.12.006

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