Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathy.
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Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillationEvidence for a gene influencing heart rate on chromosome 5p13-14 in a meta-analysis of genome-wide scans from the NHLBI Family Blood Pressure Program.Potassium channel gene mutations rarely cause atrial fibrillationImproved understanding of the pathophysiology of atrial fibrillation through the lens of discrete pathological pathwaysAtrial fibrillation in congestive heart failure.Genetics of atrial fibrillationPersonalized medicine and atrial fibrillation: will it ever happen?Mutation in the S3 segment of KCNQ1 results in familial lone atrial fibrillationMonogenic atrial fibrillation as pathophysiological paradigms.Genetics of atrial fibrillation: implications for future research directions and personalized medicine.Common and rare variants in SCN10A modulate the risk of atrial fibrillation.Rs7193343 polymorphism in zinc finger homeobox 3 (ZFHX3) gene and atrial fibrillation: an updated meta-analysis of 10 case-control comparisons.Molecular Basis of Gene-Gene Interaction: Cyclic Cross-Regulation of Gene Expression and Post-GWAS Gene-Gene Interaction Involved in Atrial Fibrillation.The Role of Pharmacogenetics in Atrial Fibrillation Therapeutics: Is Personalized Therapy in Sight?Drug therapy for atrial fibrillation: where do we go from here?Mechanisms of disease: Genetic mechanisms of atrial fibrillation.Prolonged signal-averaged P-wave duration as an intermediate phenotype for familial atrial fibrillation.Genetic mechanisms of atrial fibrillation: impact on response to treatmentMolecular genetics of atrial fibrillation.Significant association of SNP rs2106261 in the ZFHX3 gene with atrial fibrillation in a Chinese Han GeneID population.Arrhythmia pharmacogenomics: methodological considerations.Angiotensin II receptor blockers in the prevention of atrial fibrillation.Atrial fibrillation: the role of common and rare genetic variants.Genomics of Atrial Fibrillation.Lone atrial fibrillation: what is known and what is to come.2012 HRS/EHRA/ECAS expert consensus statement on catheter and surgical ablation of atrial fibrillation: recommendations for patient selection, procedural techniques, patient management and follow-up, definitions, endpoints, and research trial designGenetic Discoveries in Atrial Fibrillation and Implications for Clinical Practice.The "missing" link in atrial fibrillation heritability.Lone AF - Etiologic Factors and Genetic Insights into Pathophysiolgy.Novel connexin40 missense mutations in patients with familial atrial fibrillation.The non-synonymous coding IKr-channel variant KCNH2-K897T is associated with atrial fibrillation: results from a systematic candidate gene-based analysis of KCNH2 (HERG)
P2860
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P2860
Genome-wide linkage scan identifies a novel genetic locus on chromosome 5p13 for neonatal atrial fibrillation associated with sudden death and variable cardiomyopathy.
description
2004 nî lūn-bûn
@nan
2004 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի դեկտեմբերին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Genome-wide linkage scan ident ...... h and variable cardiomyopathy.
@ast
Genome-wide linkage scan ident ...... h and variable cardiomyopathy.
@en
type
label
Genome-wide linkage scan ident ...... h and variable cardiomyopathy.
@ast
Genome-wide linkage scan ident ...... h and variable cardiomyopathy.
@en
prefLabel
Genome-wide linkage scan ident ...... h and variable cardiomyopathy.
@ast
Genome-wide linkage scan ident ...... h and variable cardiomyopathy.
@en
P2093
P2860
P1433
P1476
Genome-wide linkage scan ident ...... h and variable cardiomyopathy.
@en
P2093
Carlos Oberti
Jiamei Dong
Lejin Wang
Shaoqi Rao
P2860
P304
P356
10.1161/01.CIR.0000150333.87176.C7
P407
P577
2004-12-13T00:00:00Z