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The N588K-HERG K+ channel mutation in the ‘short QT syndrome’: Mechanism of gain-in-function determined at 37 °C

✍ Scribed by Mark J. McPate; Rona S. Duncan; James T. Milnes; Harry J. Witchel; Jules C. Hancox

No coin nor oath required. For personal study only.

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The N588K-HERG K+ channel mutation in the ‘short QT syndrome’: Mechanism of gain-in-function determined at 37&#xa0;°C