Novel SCN5A mutation associated with multifocal ectopic purkinje-related premature contractions

被引：0
|
作者：
Holl, M. J. M. [1 ]
Verhagen, J. M. A. [2 ]
Wessels, M. W. [2 ]
Yap, S. C. [1 ]
机构：
[1] Erasmus MC, Dept Cardiol, Rotterdam, Netherlands
[2] Erasmus MC, Dept Clin Genet, Rotterdam, Netherlands
来源：
EUROPEAN HEART JOURNAL | 2018年 / 39卷
关键词：
D O I：
暂无
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
4290
引用
收藏
页码：866 / 866
页数：1
相关论文
共 50 条
  • [21] SCN5A mutation associated with a novel cardiac arrhythmia disorder involving the left fascicular-Purkinje system associated with dilated cardiomyopathy
    Laurent, G.
    Saal, S.
    Amarouch, M. Y.
    Faivre, L.
    Charron, P.
    Baron, E.
    Schott, J. J.
    Kyndt, F.
    Probst, V.
    Wolf, J. E.
    EUROPEAN HEART JOURNAL, 2010, 31 : 445 - 445
  • [22] TACHYCARDIA INDUCED CARDIOMYOPATHY ASSOCIATED TO SCN5A MUTATION
    Gonzalez, Bernardita
    Munoz, Pilar
    Parra, Claudio
    Bravo, Catherine
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2023, 81 (08) : 2623 - 2623
  • [23] A novel SCN5A mutation associated with ventricular fibrillation and left ventricular dilatation
    Wang, R.
    Li, N.
    Zhang, Y.
    Pu, J.
    EUROPEAN HEART JOURNAL, 2010, 31 : 1038 - 1038
  • [24] A Novel SCN5A Mutation Associated with Drug Induced Brugada Type ECG
    Turker, Isik
    Makiyama, Takeru
    Vatta, Matteo
    Itoh, Hideki
    Ueyama, Takeshi
    Shimizu, Akihiko
    Ai, Tomohiko
    Horie, Minoru
    PLOS ONE, 2016, 11 (08):
  • [25] A Novel SCN5A Mutation Associated With Brugada Type ECG And Intraventricular Conduction Defects
    Samani, Kaveh
    Ai, Tomohiko
    Towbin, Jeffrey A.
    Brugada, Ramon
    Xi, Yutao
    Cheng, Jie
    Vatta, Matteo
    BIOPHYSICAL JOURNAL, 2009, 96 (03) : 263A - 263A
  • [26] Novel SCN5A Frameshift Mutation in Brugada Syndrome Associated With Complex Arrhythmic Phenotype
    Micaglio, Emanuele
    Monasky, Michelle M.
    Ciconte, Giuseppe
    Vicedomini, Gabriele
    Conti, Manuel
    Mecarocci, Valerio
    Giannelli, Luigi
    Giordano, Federica
    Pollina, Alberto
    Saviano, Massimo
    Pozzi, Paolo R.
    Di Restaz, Chiara
    Benedetti, Sara
    Ferrari, Maurizio
    Santinelli, Vincenzo
    Pappone, Carlo
    FRONTIERS IN GENETICS, 2019, 10
  • [27] NOVEL SCN5A MUTATION ASSOCIATED WITH LETHAL DRUG RESISTANT LONG QT SYNDROME
    Pournamdari, Ashley
    Wang, Jessica
    Nguyen, Thao P.
    George, Alfred
    Potet, Franck
    JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2022, 79 (09) : 2521 - 2521
  • [28] Congenital atrial standstill associated with coinheritance of a novel SCN5A mutation and connexin 40 polymorphisms
    Makita, N
    Sasaki, K
    Groenewegen, WA
    Yokota, T
    Yokoshiki, H
    Murakami, T
    Tsutsui, H
    HEART RHYTHM, 2005, 2 (10) : 1128 - 1134
  • [29] Novel SCN5A mutation associated with idiopathic ventricular fibrillation due to subclinical Brugada syndrome
    Jimenez-Jaimez, Juan
    Alvarez-Lopez, Miguel
    Tercedor-Sanchez, Luis
    Santiago, Pablo
    Algarra, Maria
    Penas, Rocio
    Valverde, Francisca
    Melgares-Moreno, Rafael
    CARDIOGENETICS, 2012, 2 (01) : 1 - 5
  • [30] Molecular and Clinical Characterization of a Novel SCN5A Mutation Associated With Atrioventricular Block and Dilated Cardiomyopathy
    Ge, Junbo
    Sun, Aijun
    Paajanen, Vesa
    Wang, Shijun
    Su, Chunxi
    Yang, Zhiyin
    Li, Ying
    Wang, Shaochun
    Jia, Jianguo
    Wang, Keqiang
    Zou, Yunzeng
    Gao, Lizhi
    Wang, Kun
    Fan, Zheng
    CIRCULATION-ARRHYTHMIA AND ELECTROPHYSIOLOGY, 2008, 1 (02): : 83 - 92
12345