Investigating Arrhythmogenic Potential of a Novel KCNH2 Mutation Leading to Long QT Syndrome

Bright Tsevi,Akwasi D. Akwaboah, Jacqueline A. Treat, Robert Goodrow, Victoria Lam,Anthony Owusu-Mensah,Michel Audette,Jonathan M. Cordeiro,Makarand Deo

Circulation（2021）

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摘要

Background: Mutations in the gene KCNH2 have been associated with both Short and Long QT syndrome. In this study, we identified a 1-day old infant that exhibited T-wave alternans coupled with Long ...

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