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A founder mutation of the potassium channel KCNQ1 in long QT syndrome: Implications for estimation of disease prevalence and molecular diagnostics

✍ Scribed by Kirsi Piippo; Heikki Swan; Michael Pasternack; Hugh Chapman; Kristian Paavonen; Matti Viitasalo; Lauri Toivonen; Kimmo Kontula

No coin nor oath required. For personal study only.

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