- Genetic Mutation in Korean Patients of Sudden Cardiac Arrest as a Surrogating Marker of Idiopathic Ventricular Arrhythmia
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Son MK, Ki CS, Park SJ, Huh J, Kim JS, On YK
- KMID: 1777497
- J Korean Med Sci.
- 2013 Jul;28(7):1021-1026.
- doi: 10.3346/jkms.2013.28.7.1021
Mutation or common intronic variants in cardiac ion channel genes have been suggested to be associated with sudden cardiac death caused by idiopathic ventricular tachyarrhythmia. This study aimed to find... -
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- Long QT Syndrome: a Korean Single Center Study
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Lee YS, Kwon BS, Kim GB, Oh SI, Bae EJ, Park SS, Noh CI
- KMID: 1777681
- J Korean Med Sci.
- 2013 Oct;28(10):1454-1460.
- doi: 10.3346/jkms.2013.28.10.1454
The long QT syndrome (LQTS) is a rare hereditary disorder in which affected individuals have a possibility of ventricular tachyarrhythmia and sudden cardiac death. We investigated 62 LQTS (QTc >... -
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- Genetic Analysis of SCN5A in Korean Patients Associated with Atrioventricular Conduction Block
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Park HS, Kim YN, Lee YS, Jung BC, Lee SH, Shin DG, Cho Y, Bae MH, Han SM, Lee MH
- KMID: 2166493
- Genomics Inform.
- 2012 Jun;10(2):110-116.
- doi: 10.5808/GI.2012.10.2.110
Recent several studies have shown that the genetic variation of SCN5A is related with atrioventricular conduction block (AVB); no study has yet been published in Koreans. Therefore, to determine the... -
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