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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Detalhes bibliográficos
Publicado no:J Cardiol Cases
Main Authors: 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
Formato: Artigo
Idioma:Inglês
Publicado em: Japanese College of Cardiology 2012
Assuntos:
Case Report
Acesso em linha: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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