Associated Papers
Identification of novel genetic risk factors of dilated cardiomyopathy: from canine to human.
Niskanen JE et al.
Genome Medicine, 2023
37723491 (PubMed )
Supplement: 13073_2023_1221_MOESM2_ESM.xlsx › Table_S17
Rare variants of small effect size in neuronal excitability genes influence clinical outcome in Japanese cases of SCN1A truncation-positive Dravet syndrome.
Hammer MF et al.
Plos One, 2017
28686619 (PubMed )
Supplement: pone.0180485.s008.xlsx › Sheet1
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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