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- W1982103659 abstract "KCNJ2 is the only gene implicated in Andersen-Tawil syndrome. Sudden cardiac arrest is rare in Andersen-Tawil syndrome. However, sudden cardiac arrest is often the index presentation in other forms of long QT syndrome. We present an unreported variant in the KCNJ2 gene, associated with long QT syndrome, that presented with ventricular fibrillation. Exercise testing and adrenaline infusion were useful in assigning pathogenicity to this variant of unknown significance." @default.
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- W1982103659 date "2011-11-01" @default.
- W1982103659 modified "2023-09-24" @default.
- W1982103659 title "KCNJ2 Variant of Unknown Significance Reclassified as Long QT Syndrome Causing Ventricular Fibrillation" @default.
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- W1982103659 doi "https://doi.org/10.1016/j.cjca.2011.05.004" @default.
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