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3. Atrial Fibrillation
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5. Nkx2.5/CARP signaling pathway contributes to the regulation of ion channel remodeling induced by rapid pacing in rat atrial myocytes
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6. Genetics of Atrial Fibrilation: In Search of Novel Therapeutic Targets
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7. TBX5 loss-of-function mutation contributes to atrial fibrillation and atypical Holt-Oram syndrome
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8. Homeobox Genes and Homeodomain Proteins: New Insights into Cardiac Development, Degeneration and Regeneration
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10. A novel TBX5 loss-of-function mutation associated with sporadic dilated cardiomyopathy
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11. Genetics of Atrial Fibrillation
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12. Epidemiology of Atrial Fibrillation
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13. Atrial fibrillation
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14. Prevalence and spectrum of NKX2.5 mutations in patients with congenital atrial septal defect and atrioventricular block
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15. NKX2‐6 related congenital heart disease: Biallelic homeodomain‐disrupting variants and truncus arteriosus
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16. Novel Gene Polymorphisms for Stable Warfarin Dose in a Korean Population: Genome-Wide Association Study
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17. Genetics of atrial fibrillation: from families to genomes
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18. Integrated transcriptomics and epigenomics reveal chamber-specific and species-specific characteristics of human and mouse hearts
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19. Mechanisms of Atrial Fibrillation: How Our Knowledge Affects Clinical Practice
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20. Novel missense mutation in NKX2.6 gene (c.389 G > C, Arg130Pro) as a potentially pathogenic variant in pediatric patients with congenital heart disease
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