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Title
Whole-exome sequencing in familial atrial fibrillation
Authors
Keywords
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Journal
EUROPEAN HEART JOURNAL
Volume 35, Issue 36, Pages 2477-2483
Publisher
Oxford University Press (OUP)
Online
2014-04-12
DOI
10.1093/eurheartj/ehu156
References
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Related references
Note: Only part of the references are listed.- Exome Sequencing and Systems Biology Converge to Identify Novel Mutations in the L-Type Calcium Channel, CACNA1C , Linked to Autosomal Dominant Long QT Syndrome
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- Evaluating Pathogenicity of Rare Variants From Dilated Cardiomyopathy in the Exome Era
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- Chromosome 4q25 Variants Are Genetic Modifiers of Rare Ion Channel Mutations Associated With Familial Atrial Fibrillation
- (2012) Marylyn D. Ritchie et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Differential confounding of rare and common variants in spatially structured populations
- (2012) Iain Mathieson et al. NATURE GENETICS
- Meta-analysis identifies six new susceptibility loci for atrial fibrillation
- (2012) Patrick T Ellinor et al. NATURE GENETICS
- Exome sequencing as a tool for Mendelian disease gene discovery
- (2011) Michael J. Bamshad et al. NATURE REVIEWS GENETICS
- Systems Pharmacology of Arrhythmias
- (2010) S. I. Berger et al. Science Signaling
- Transgenic simulation of human heart failure-like L-type Ca2+-channels: implications for fibrosis and heart rate in mice
- (2009) Nadine Beetz et al. CARDIOVASCULAR RESEARCH
- Accelerated inactivation of the L-type calcium current due to a mutation in CACNB2b underlies Brugada syndrome
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- Finding the missing heritability of complex diseases
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- Exome sequencing identifies the cause of a mendelian disorder
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- Prolonged Signal-Averaged P-Wave Duration as an Intermediate Phenotype for Familial Atrial Fibrillation
- (2008) Dawood Darbar et al. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
- Atrial Natriuretic Peptide Frameshift Mutation in Familial Atrial Fibrillation
- (2008) Denice M. Hodgson-Zingman et al. NEW ENGLAND JOURNAL OF MEDICINE
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