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- W2026523610 abstract "The long QT syndrome is characterized by prolongation of the cardiac action potential resulting in increased heterogeneity of repolarization and early afterdepolarizations, which trigger the life-threatening ventricular arrhythmia torsades de pointes. Advances in understanding the specific ion channel-related gene mutations linked to the congenital long QT syndrome and mechanisms underlying the acquired long QT syndrome are described, along with emerging technologies to study these diseases." @default.
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- W2026523610 date "2004-10-01" @default.
- W2026523610 modified "2023-10-14" @default.
- W2026523610 title "Inherited and acquired long QT syndromes: new insights and evolving technology" @default.
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- W2026523610 doi "https://doi.org/10.1016/j.ddmec.2004.08.014" @default.
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