Brugada syndrome risk loci seem protective against atrial fibrillation. - Wikidata - wikimedia - TriplyDB

Brugada syndrome risk loci seem protective against atrial fibrillation.

Brugada syndrome risk loci seem protective against atrial fibrillation.

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The Brugada Syndrome: A Rare Arrhythmia Disorder with Complex Inheritance The Role of Pharmacogenetics in Atrial Fibrillation Therapeutics: Is Personalized Therapy in Sight?Genetic Discoveries in Atrial Fibrillation and Implications for Clinical Practice.Brugada Syndrome-Associated Genetic Loci Are Associated With J-Point Elevation and an Increased Risk of Cardiac Arrest

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Brugada syndrome risk loci seem protective against atrial fibrillation.

http://www.wikidata.org/entity/Q34508291

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2014 nî lūn-bûn

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2014 թուականի Մարտին հրատարակուած գիտական յօդուած

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2014 թվականի մարտին հրատարակված գիտական հոդված

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2014年の論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年論文

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2014年论文

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name

Brugada syndrome risk loci seem protective against atrial fibrillation.

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Brugada syndrome risk loci seem protective against atrial fibrillation.

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Brugada syndrome risk loci seem protective against atrial fibrillation.

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label

Brugada syndrome risk loci seem protective against atrial fibrillation.

@ast

Brugada syndrome risk loci seem protective against atrial fibrillation.

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Brugada syndrome risk loci seem protective against atrial fibrillation.

@nl

prefLabel

Brugada syndrome risk loci seem protective against atrial fibrillation.

@ast

Brugada syndrome risk loci seem protective against atrial fibrillation.

@en

Brugada syndrome risk loci seem protective against atrial fibrillation.

@nl

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European Journal of Human Genetics

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Brugada syndrome risk loci seem protective against atrial fibrillation.

@en

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Arnljot Tveit

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Javad Jabbari

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Jens J Thiis

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Jonas B Nielsen

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Laura Andreasen

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Stig Haunsø

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Stine Darkner

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P2860

Somatic mutations in the connexin 40 gene (GJA5) in atrial fibrillation

A novel nonsense variant in Nav1.5 cofactor MOG1 eliminates its sodium current increasing effect and may increase the risk of arrhythmias

Mutations in sodium channel β-subunit SCN3B are associated with early-onset lone atrial fibrillation

Genetic variation in KCNA5: impact on the atrial-specific potassium current IKur in patients with lone atrial fibrillation

Augmented potassium current is a shared phenotype for two genetic defects associated with familial atrial fibrillation

Hey basic helix-loop-helix transcription factors are repressors of GATA4 and GATA6 and restrict expression of the GATA target gene ANF in fetal hearts

Gain-of-function mutation S422L in the KCNJ8-encoded cardiac K(ATP) channel Kir6.1 as a pathogenic substrate for J-wave syndromes

Common variants at SCN5A-SCN10A and HEY2 are associated with Brugada syndrome, a rare disease with high risk of sudden cardiac death

2011 ACCF/AHA/HRS Focused Updates Incorporated Into the ACC/AHA/ESC 2006 Guidelines for the Management of Patients With Atrial Fibrillation

CHF1/Hey2 plays a pivotal role in left ventricular maturation through suppression of ectopic atrial gene expression

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1357-1361

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10.1038/EJHG.2014.46

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12

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22

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Jesper Hastrup Svendsen

Morten Salling Olesen

Ingrid Christophersen

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2014-03-26T00:00:00Z

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261103435

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24667784

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