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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 |
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| Authors: | Fodstad Heidi Swan Heikki Laitinen Päivi Piippo Kirsi Paavonen Kristian Viitasalo Matti Toivonen Lauri Kontula Kimmo |
| Affiliation: | Research Program in Molecular Medicine, Biomedicum Helsinki, Finland. |
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| 本文献已被 PubMed 等数据库收录！ | |