Four potassium channel mutations account for 73% of the genetic spectrum underlying long-QT syndrome (LQTS) and provide evidence for a strong founder effect in Finland

Author: Fodstad Heidi   Swan Heikki   Laitinen Päivi   Piippo Kirsi   Paavonen Kristian   Viitasalo Matti   Toivonen Lauri   Kontula Kimmo  

Publisher: Informa Healthcare

ISSN: 0785-3890

Source: Annals of Medicine, Vol.36, Iss.1, 2004-05, pp. : 53-63

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