Temporal repolarization lability differences among genotyped patients with the long QT syndrome-Reference-Cited by-同舟云学术

Temporal repolarization lability differences among genotyped patients with the long QT syndrome

Published:2004-11 Issue:10 Volume:94 Page:1312-1316
ISSN:0002-9149
Container-title:The American Journal of Cardiology
language:en
Short-container-title:The American Journal of Cardiology

Author:

Bilchick Kenneth,Viitasalo Matti,Oikarinen Lasse,Fetics Barry,Tomaselli Gordon,Swan Heikki,Laitinen P.äivi J.,Väänänen Heikki,Kontula Kimmo,Berger Ronald D.

Publisher

Elsevier BV

Subject

Cardiology and Cardiovascular Medicine

Reference16 articles.

1. A founder mutation of the potassium channel KCNQ1 in long QT syndrome: implications for estimation of disease prevalence and molecular diagnostics;Piippo;J Am Coll Cardiol,2001

2. Molecular genetics of the long QT syndrome: two novel mutations of the KVLQT1 gene and phenotypic expression of the mutant gene in a large kindred;Saarinen;Hum Mutat,1998

3. Genomic organization of the KCNQ1 K+ channel gene and identification of C-terminal mutations in the long-QT syndrome;Neyroud;Circ Res,1999

4. Survey of the coding region of the HERG gene in long QT syndrome reveals six novel mutations and an amino acid polymorphism with possible phenotypic effects;Laitinen;Hum Mutat,2000

5. Homozygosity for a HERG potassium channel mutation causes a severe form of long QT syndrome: identification of an apparent founder mutation in the Finns;Piippo;J Am Coll Cardiol,2000

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