p.Y1449C SCN5A mutation associated with overlap disorder comprising conduction disease, Brugada syndrome, and atrial flutter.
about
Conduction abnormalities and ventricular arrhythmogenesis: The roles of sodium channels and gap junctionsElectrophysiological Mechanisms of Brugada Syndrome: Insights from Pre-clinical and Clinical StudiesAtrial arrhythmias in inherited arrhythmogenic disordersBrugada syndrome in children - Stepping into unchartered territory.Critical Roles of Xirp Proteins in Cardiac Conduction and Their Rare Variants Identified in Sudden Unexplained Nocturnal Death Syndrome and Brugada Syndrome in Chinese Han Population.Association of common and rare variants of SCN10A gene with sudden unexplained nocturnal death syndrome in Chinese Han population.
P2860
p.Y1449C SCN5A mutation associated with overlap disorder comprising conduction disease, Brugada syndrome, and atrial flutter.
description
2014 nî lūn-bûn
@nan
2014 թուականի Յուլիսին հրատարակուած գիտական յօդուած
@hyw
2014 թվականի հուլիսին 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
p.Y1449C SCN5A mutation associ ...... syndrome, and atrial flutter.
@ast
p.Y1449C SCN5A mutation associ ...... syndrome, and atrial flutter.
@en
type
label
p.Y1449C SCN5A mutation associ ...... syndrome, and atrial flutter.
@ast
p.Y1449C SCN5A mutation associ ...... syndrome, and atrial flutter.
@en
prefLabel
p.Y1449C SCN5A mutation associ ...... syndrome, and atrial flutter.
@ast
p.Y1449C SCN5A mutation associ ...... syndrome, and atrial flutter.
@en
P2093
P2860
P356
P1476
p.Y1449C SCN5A mutation associ ...... syndrome, and atrial flutter.
@en
P2093
Farhana Ara
Jonathan Timperley
Sandeep S Hothi
P2860
P356
10.1111/JCE.12470
P577
2014-07-23T00:00:00Z