about
Emerging directions in the genetics of atrial fibrillationNovel GATA6 mutations associated with congenital ventricular septal defect or tetralogy of fallotGATA5 loss-of-function mutations underlie tetralogy of fallot.Prevalence and spectrum of Nkx2.5 mutations associated with idiopathic atrial fibrillation.PITX2C loss-of-function mutations responsible for idiopathic atrial fibrillation.Atrial fibrillation: the role of common and rare genetic variants.Mutational spectrum of the NKX2-5 gene in patients with lone atrial fibrillationGATA-dependent transcriptional and epigenetic control of cardiac lineage specification and differentiation.Genetic Discoveries in Atrial Fibrillation and Implications for Clinical Practice.
P2860
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P2860
description
2012 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2012 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
artículu científicu espublizáu en 2012
@ast
scientific journal article
@en
wetenschappelijk artikel (gepubliceerd op 2012/10/01)
@nl
наукова стаття, опублікована в жовтні 2012
@uk
مقالة علمية (نشرت في أكتوبر 2012)
@ar
name
GATA6 loss-of-function mutation in atrial fibrillation
@ast
GATA6 loss-of-function mutation in atrial fibrillation
@en
type
label
GATA6 loss-of-function mutation in atrial fibrillation
@ast
GATA6 loss-of-function mutation in atrial fibrillation
@en
prefLabel
GATA6 loss-of-function mutation in atrial fibrillation
@ast
GATA6 loss-of-function mutation in atrial fibrillation
@en
P2093
P921
P1476
GATA6 loss-of-function mutation in atrial fibrillation
@en
P2093
Hong-Wei Tan
Jin-Qi Jiang
Wei-Yi Fang
Xian-Ling Zhang
Xin-Hua Wang
Yi-Qing Yang
P304
P356
10.1016/J.EJMG.2012.06.007
P577
2012-10-01T00:00:00Z