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A novel PITX2c loss-of-function mutation underlies lone atrial fibrillation

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Evaluation of non-synonymous NPPA single nucleotide polymorphisms in atrial fibrillation

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Genetic Variants Related to Height and Risk of Atrial Fibrillation

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Gain-of-function mutations in GATA6 lead to atrial fibrillation

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Ion channel dysfunction and fibrosis in atrial fibrillation: Two sides of the same coin

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NKX2-6 mutation predisposes to familial atrial fibrillation

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Genetic Variants Associated With Susceptibility to Atrial Fibrillation in a Japanese Population

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Connexin Remodeling Contributes to Atrial Fibrillation.

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Can We Predict the Occurrence of Atrial Fibrillation?

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