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Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns

✍ Scribed by Kirsi Piippo; Päivi Laitinen; Heikki Swan; Lauri Toivonen; Matti Viitasalo; Michael Pasternack; Kristian Paavonen; Hugh Chapman; Kenneth T. Wann; Eeva Hirvelä; Antti Sajantila; Kimmo Kontula

Book ID: 119541505
Publisher: Elsevier Science
Year: 2000
Tongue: English
Weight: 320 KB
Volume: 35
Category: Article
ISSN: 1558-3597
DOI: 10.1016/s0735-1097(00)00636-7

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