Authors:
Piippo, K
Laitinen, P
Swan, H
Toivonen, L
Viitasalo, M
Pasternack, M
Paavonen, K
Chapman, H
Wann, KT
Hirvela, E
Sajantila, A
Kontula, K
Citation: K. Piippo et al., Homozygosity for a HERG potassium channel mutation causes a severe form oflong-QT syndrome: Identification of an apparent founder mutation in the Finns, J AM COL C, 35(7), 2000, pp. 1919-1925