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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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  3. Aborted Cardiac Arrest in LQT2 Related to Novel KCNH2 (hERG) Variant Identified in One Lithuanian Family
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  5. Gene- and variant-specific efficacy of serum/glucocorticoid-regulated kinase 1 inhibition in long QT syndrome types 1 and 2
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  7. KCNH2A561V Heterozygous Mutation Inhibits KCNH2 Protein Expression via The Activation of UPR Mediated by ATF6
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  8. Venom-derived peptide inhibitors of voltage-gated potassium channels
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  9. Stop codons and the +4 nucleotide may influence the efficiency of G418 in rescuing nonsense mutations of the HERG gene
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  10. The ERG1 K+ Channel and Its Role in Neuronal Health and Disease
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  11. Identifying and Analyzing Novel Epilepsy-Related Genes Using Random Walk with Restart Algorithm
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  13. F463L increases the potential of dofetilide on human ether‐a‐go‐go‐related gene (hERG) channels
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  14. Estimating the Posttest Probability of Long QT Syndrome Diagnosis for Rare KCNH2 Variants
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