A case of long QT syndrome having compound mutations of KCNH2 and SCN5A

Long QT syndrome (LQTS) is a hereditary ion channelopathy resulting in prolonged cardiac repolarization and abnormal prolongation of the QT interval on the electrocardiogram (ECG). The patients are likely to develop ventricular arrhythmias and sudden cardiac death. Molecular biology and basic electr...

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Dettagli Bibliografici
Pubblicato in:J Cardiol Cases
Autori principali: Ito, Saki, Taketani, Takeshi, Sugamori, Takashi, Okada, Taiji, Sato, Hirotomo, Adachi, Tomoko, Takeda, Masaki, Kodani, Nobuhiro, Takahashi, Nobuyuki, Endo, Akihiro, Yoshitomi, Hiroyuki, Tanabe, Kazuaki, Shimizu, Wataru
Natura: Artigo
Lingua:Inglês
Pubblicazione: Japanese College of Cardiology 2012
Soggetti:
Case Report
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC6269416/
https://ncbi.nlm.nih.gov/pubmed/30533098
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.jccase.2012.07.004
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