KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death-Reference-Cited by-同舟云学术

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KCNQ1 mutations in patients with a family history of lethal cardiac arrhythmias and sudden death

Published:2003-04 Issue:4 Volume:63 Page:273-282
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:

Author:

Chen S,Zhang L,Bryant RM,Vincent GM,Flippin M,Lee JC,Brown E,Zimmerman F,Rozich R,Szafranski P,Oberti C,Sterba R,Marangi D,Tchou PJ,Chung MK,Wang Q

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1399-0004.2003.00048.x/fullpdf

Reference29 articles.

1. A new familial cardiac syndrome in children;Ward;J Ir Med Assoc,1964

2. Congenital cardiac arrhythmia;Romano;Lancet,1965

3. Congenital deaf mutism, functional heart disease with prolongation of the QT interval, and sudden death;Jervell;Am Heart J,1957

4. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias;Wang;Nature Genet,1996

5. K(v)LQT1 and IsK (mink) associate to form the I (ks) cardiac potassium current;Barhanin;Nature Proteins,1996

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