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2. A novel GATA5 loss-of-function mutation underlies lone atrial fibrillation
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3. Novel GATA6 loss-of-function mutation responsible for familial atrial fibrillation
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4. The Connexin40A96S mutation from a patient with atrial fibrillation causes decreased atrial conduction velocities and sustained episodes of induced atrial fibrillation in mice
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8. A novel NKX2.5 loss-of-function mutation responsible for familial atrial fibrillation
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13. Copy Number Variants of Undetermined Significance Are Not Associated with Worse Clinical Outcomes in Hypoplastic Left Heart Syndrome
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18. The rs2236609 Polymorphism Is Related to Increased Risk Susceptibility of Atrial Fibrillation
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19. Research Progress on Natural Products’ Therapeutic Effects on Atrial Fibrillation by Regulating Ion Channels
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20. Connexinplexity: the spatial and temporal expression of connexin genes during vertebrate organogenesis
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