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• W2411094836 abstract "Genetic cardiac diseases related to potassium channelopathies are a group of relatively rare syndromes that includes long QT syndrome, short QT syndrome, Brugada syndrome, and early repolarization syndrome. Patients with these syndromes share a propensity for the development of life-threatening ventricular arrhythmias in the absence of significant cardiac structural abnormalities. Familial atrial fibrillation has also been associated with potassium channel dysfunction but differs from the other syndromes by being a rare cause of a common condition. This article focuses on the clinical features, diagnosis, and management of these syndromes." @default.
• W2411094836 created "2016-06-24" @default.
• W2411094836 creator A5002978899 @default.
• W2411094836 creator A5024543642 @default.
• W2411094836 date "2016-06-01" @default.
• W2411094836 modified "2023-09-26" @default.
• W2411094836 title "Clinical Features of Genetic Cardiac Diseases Related to Potassium Channelopathies" @default.
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• W2411094836 doi "https://doi.org/10.1016/j.ccep.2016.02.001" @default.
• W2411094836 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/27261827" @default.
• W2411094836 hasPublicationYear "2016" @default.
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