1. Computational analysis of the effect of KCNH2 L532P mutation on ventricular electromechanical behaviors
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2. Targeted next generation sequencing revealed a novel deletion-frameshift mutation of KCNH2 gene in a Chinese Han family with long QT syndrome
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6. KCNH2A561V Heterozygous Mutation Inhibits KCNH2 Protein Expression via The Activation of UPR Mediated by ATF6
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7. Venom-derived peptide inhibitors of voltage-gated potassium channels
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8. Stop codons and the +4 nucleotide may influence the efficiency of G418 in rescuing nonsense mutations of the HERG gene
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9. The ERG1 K+ Channel and Its Role in Neuronal Health and Disease
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10. Identifying and Analyzing Novel Epilepsy-Related Genes Using Random Walk with Restart Algorithm
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12. F463L increases the potential of dofetilide on human ether‐a‐go‐go‐related gene (hERG) channels
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13. Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants
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14. Pharmacological corrections of the mutant hERG channels by posaconazole
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