A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation.
about
Atrial Fibrillation and SCN5A Variants.The genetic basis for inherited forms of sinoatrial dysfunction and atrioventricular node dysfunctionCardiac sodium channel regulator MOG1 regulates cardiac morphogenesis and rhythm.Building a family network from genetic testing.Calmodulin limits pathogenic Na+ channel persistent current.Voltage-gated sodium channels assemble and gate as dimers.Infant sudden death: Mutations responsible for impaired Nav1.5 channel trafficking and function.Inhibitory effects of neferine on Nav1.5 channels expressed in HEK293 cells.Sinus Bradycardia in Carriers of the SCN5A-1795insD Mutation: Unraveling the Mechanism through Computer Simulations.The voltage-gated sodium channel EF-hands form an interaction with the III-IV linker that is disturbed by disease-causing mutations.Disease Modifiers of Inherited Channelopathy
P2860
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P2860
A truncating SCN5A mutation combined with genetic variability causes sick sinus syndrome and early atrial fibrillation.
description
2014 nî lūn-bûn
@nan
2014 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2014年の論文
@ja
2014年論文
@yue
2014年論文
@zh-hant
2014年論文
@zh-hk
2014年論文
@zh-mo
2014年論文
@zh-tw
2014年论文
@wuu
name
A truncating SCN5A mutation co ...... and early atrial fibrillation.
@ast
A truncating SCN5A mutation co ...... and early atrial fibrillation.
@en
type
label
A truncating SCN5A mutation co ...... and early atrial fibrillation.
@ast
A truncating SCN5A mutation co ...... and early atrial fibrillation.
@en
prefLabel
A truncating SCN5A mutation co ...... and early atrial fibrillation.
@ast
A truncating SCN5A mutation co ...... and early atrial fibrillation.
@en
P2093
P2860
P50
P1433
P1476
A truncating SCN5A mutation co ...... and early atrial fibrillation
@en
P2093
Alain Coulombe
Azza Ziyadeh-Isleem
Isabelle Denjoy
Isabelle Deschênes
Jérôme Clatot
Sabine Duchatelet
P2860
P304
P356
10.1016/J.HRTHM.2014.02.021
P577
2014-02-25T00:00:00Z