- Single Nucleotide Deletion Mutation of KCNH2 Gene is Responsible for LQT Syndrome in a 3-Generation Korean Family
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Park JK, Oh YS, Choi JH, Yoon SK
- KMID: 1793058
- J Korean Med Sci.
- 2013 Sep;28(9):1388-1393.
- doi: 10.3346/jkms.2013.28.9.1388
Long QT syndrome (LQTS) is characterized by the prolongation of the QT interval in ECG and manifests predisposition to life threatening arrhythmia which often leads to sudden cardiac death. We... -
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