Associated Papers
Coexistent HCN4 and GATA5 Rare Variants and Atrial Fibrillation in a Large Spanish Family.
Fraile A et al.
The Canadian Journal of Cardiology, 2024
Familial Paralysis of the Atrium Due to a Mutation in SCN5A.
Robles C et al.
Revista Espanola De Cardiologia (english Ed.), 2015
Pacemaker activity of the human sinoatrial node: an update on the effects of mutations in HCN4 on the hyperpolarization-activated current.
Verkerk AO et al.
International Journal of Molecular Sciences, 2015
A novel trafficking-defective HCN4 mutation is associated with early-onset atrial fibrillation.
Macri V et al.
Heart Rhythm, 2014
HCN4 and arrhythmias: Insights into base mutations.
Fan W et al.
Mutation Research. Reviews in Mutation Research, 0
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