Molecular basis of congenital and acquired long QT syndromes

被引:16
作者
Ackerman, MJ [1 ]
机构
[1] Mayo Clin & Mayo Fdn, Long QT Syndrome Clin & Sudden Death Genom Lab, Dept Med Pediat & Mol Pharmacol, Rochester, MN 55905 USA
关键词
D O I
10.1016/j.jelectrocard.2004.08.002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
引用
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页码:1 / 6
页数:6
相关论文
共 44 条
[31]   Cardiac conduction defects associate with mutations in SCN5A [J].
Schott, JJ ;
Alshinawi, C ;
Kyndt, F ;
Probst, V ;
Hoorntje, TM ;
Hulsbeek, M ;
Wilde, AAM ;
Escande, D ;
Mannens, MMAM ;
Le Marec, H .
NATURE GENETICS, 1999, 23 (01) :20-21
[32]  
SCHOTT JJ, 1995, AM J HUM GENET, V57, P1114
[33]   KCNE1 mutations cause Jervell and Lange-Nielsen syndrome [J].
SchulzeBahr, E ;
Wang, Q ;
Wedekind, H ;
Haverkamp, W ;
Chen, QY ;
Sun, YL ;
Rubie, C ;
Hordt, M ;
Towbin, JA ;
Borggrefe, M ;
Assmann, G ;
Qu, XD ;
Somberg, JC ;
Breithardt, G ;
Oberti, C ;
Funke, H .
NATURE GENETICS, 1997, 17 (03) :267-268
[34]  
Schwartz PJ, 2001, CIRCULATION, V103, P89
[35]   Epinephrine unmasks latent mutation carriers with LQT1 form of congenital long-QT syndrome [J].
Shimizu, W ;
Noda, T ;
Takaki, H ;
Kurita, T ;
Nagaya, N ;
Satomi, K ;
Suyama, K ;
Aihara, N ;
Kamakura, S ;
Sunagawa, K ;
Echigo, S ;
Nakamura, K ;
Ohe, T ;
Towbin, JA ;
Napolitano, C ;
Priori, SG .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2003, 41 (04) :633-642
[36]   Spectrum of mutations in long-QT syndrome genes KVLQT1, HERG, SCN5A, KCNE1, and KCNE2 [J].
Splawski, I ;
Shen, JX ;
Timothy, KW ;
Lehmann, MH ;
Priori, S ;
Robinson, JL ;
Moss, AJ ;
Schwartz, PJ ;
Towbin, JA ;
Vincent, GM ;
Keating, MT .
CIRCULATION, 2000, 102 (10) :1178-1185
[37]   Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia [J].
Splawski, I ;
Timothy, KW ;
Tateyama, M ;
Clancy, CE ;
Malhotra, A ;
Beggs, AH ;
Cappuccio, FP ;
Sagnella, GA ;
Kass, RS ;
Keating, MT .
SCIENCE, 2002, 297 (5585) :1333-1336
[38]   Mutations in the hminK gene cause long QT syndrome and suppress I-Ks function [J].
Splawski, I ;
TristaniFirouzi, M ;
Lehmann, MH ;
Sanguinetti, MC ;
Keating, MT .
NATURE GENETICS, 1997, 17 (03) :338-340
[39]   Molecular basis of the long-QT syndrome associated with deafness [J].
Splawski, I ;
Timothy, KW ;
Vincent, GM ;
Atkinson, DL ;
Keating, MT .
NEW ENGLAND JOURNAL OF MEDICINE, 1997, 336 (22) :1562-1567
[40]   SCN5A MUTATIONS ASSOCIATED WITH AN INHERITED CARDIAC-ARRHYTHMIA, LONG QT SYNDROME [J].
WANG, Q ;
SHEN, JX ;
SPLAWSKI, I ;
ATKINSON, D ;
LI, ZZ ;
ROBINSON, JL ;
MOSS, AJ ;
TOWBIN, JA ;
KEATING, MT .
CELL, 1995, 80 (05) :805-811