Novel gain of function SCN5A mutation causes familial atrial fibrillation

被引:0
|
作者
Rutberg, Julie [1 ]
Huang, Hai [2 ]
Lemery, Robert [1 ]
Tang, Anthony [1 ]
Birnie, David [1 ]
Green, Martin [1 ]
Lam, B. Khanh [1 ]
Roberts, Robert [1 ]
Chahine, Mohamed [2 ]
Gollob, Michael [1 ]
机构
[1] Univ Ottawa, Inst Heart, Ottawa, ON K1N 6N5, Canada
[2] Univ Laval, Quebec City, PQ G1K 7P4, Canada
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
引用
收藏
页码:54 / 54
页数:1
相关论文
共 50 条
  • [21] Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation
    Darbar, Dawood
    Kannankeril, Prince J.
    Donahue, Brian S.
    Kucera, Gayle
    Stubblefield, Tanya
    Haines, Jonathan L.
    George, Alfred L., Jr.
    Roden, Dan M.
    [J]. CIRCULATION, 2008, 117 (15) : 1927 - 1935
  • [22] Cardiac sodium channel (SCN5A) variants associated with atrial fibrillation
    Estes, N. A. Mark, III
    [J]. HEART RHYTHM, 2008, 5 (07) : 1090 - 1090
  • [23] 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
    [J]. CARDIOGENETICS, 2012, 2 (01) : 1 - 5
  • [24] 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
    [J]. HEART RHYTHM, 2005, 2 (10) : 1128 - 1134
  • [25] A common SCN5A polymorphism modulates the biophysical effects of an SCN5A mutation
    Viswanathan, PC
    Benson, DW
    Balser, JR
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2003, 111 (03): : 341 - 346
  • [26] A homozygous SCN5A mutation associated with atrial standstill and sudden death
    Tan, Reina Bianca
    Gando, Ivan
    Bu, Lei
    Cecchin, Frank
    Coetzee, William
    [J]. PACE-PACING AND CLINICAL ELECTROPHYSIOLOGY, 2018, 41 (08): : 1036 - 1042
  • [27] SCN5A mutation associated with cardiac conduction defect and atrial arrhythmias
    Laitinen-Forsblom, PJ
    Mäkynen, P
    Mäkynen, H
    Yli-Mäyry, S
    Virtanen, V
    Kontula, K
    Aalto-Setälä, K
    [J]. JOURNAL OF CARDIOVASCULAR ELECTROPHYSIOLOGY, 2006, 17 (05) : 480 - 485
  • [28] A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation
    Xia, M
    Jin, QF
    Bendahhou, S
    He, YS
    Larroque, MM
    Chen, YP
    Zhou, QS
    Yang, YQ
    Liu, Y
    Liu, B
    Zhu, Q
    Zhou, YT
    Lin, J
    Liang, B
    Li, L
    Dong, XJ
    Pan, ZW
    Wang, RG
    Wan, HY
    Qiu, WQ
    Xu, WY
    Eurlings, P
    Barhanin, J
    Chen, YH
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2005, 332 (04) : 1012 - 1019
  • [29] KCNQ1 gain-of-function mutation associated with familial atrial fibrillation
    Darbar, Dawood
    Abraham, Robert
    Kucera, Gayle
    Stubblefield, Tanya
    Yang, Tao
    Roden, Dan M.
    [J]. CIRCULATION, 2007, 116 (16) : 652 - 652
  • [30] A novel mutation in the SCN5A gene is associated with Brugada syndrome
    Shin, Dong-Jik
    Kim, Eunmin
    Park, Sang-Bum
    Jang, Won-Cheoul
    Bae, Yoonsun
    Han, Jihye
    Jang, Yangsoo
    Joung, Boyoung
    Lee, Moon Hyoung
    Kim, Sung Soon
    Huang, Hai
    Chahine, Mohamed
    Yoon, Sungjoo Kim
    [J]. LIFE SCIENCES, 2007, 80 (08) : 716 - 724