A founder mutation of the potassium channel KCNQ1 in long QT syndrome-Reference-Cited by-同舟云学术

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A founder mutation of the potassium channel KCNQ1 in long QT syndrome

Published:2001-02 Issue:2 Volume:37 Page:562-568
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,Swan Heikki,Pasternack Michael,Chapman Hugh,Paavonen Kristian,Viitasalo Matti,Toivonen Lauri,Kontula Kimmo

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference35 articles.

1. Idiopathic long QT syndrome;Schwartz;Am Heart J,1985

2. The long QT syndrome. Prospective longitudinal study of 328 families;Moss;Circulation,1991

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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