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1. Dissecting the associations of KCNH2 genetic polymorphisms with various types of cardiac arrhythmias…
2. Functional and clinical characterization of a novel homozygous KCNH2 missense variant in the pore re…
3. Identification and characterization of two novel KCNH2 mutations contributing to long QT syndrome.
4. Clinical interpretation of KCNH2 variants using a robust PS3/BS3 functional patch-clamp assay.
5. Detection of a novel pathogenic variant in KCNH2 associated with long QT syndrome 2 using whole exom…

1. Mutation-specific Therapy for the Long QT Syndrome