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
- 期刊名称Annals of Medicine
- 作者Fodstad, Heidi; Swan, Heikki; Laitinen, Päivi; Piippo, Kirsi; Paavonen, Kristian; Viitasalo, Matti; Toivonen, Lauri; Kontula, Kimmo
- 卷第36卷
- 印刷ISSN0785-3890
- 电子ISSN1365-2060
- 文件大小518.81KB
- 发表时间2004-01
- DOI10.1080/17431380410032689
- 页码53-63
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