Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns-Reference-Cited by-同舟云学术

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

Published:2000-06 Issue:7 Volume:35 Page:1919-1925
ISSN:0735-1097
Container-title:Journal of the American College of Cardiology
language:en
Short-container-title:Journal of the American College of Cardiology

Author:

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

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference33 articles.

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3. Congenital cardiac arrhythmia;Romano;Lancet,1965

4. New familial cardiac syndrome in children;Ward;J Ir Med Assoc,1964

5. Congenital deaf mutism, functional heart disease with prolongation of the Q-T interval, and sudden death;Jervell;Am Heart J,1957

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