A cardiac sodium channel mutation associated with epinephrine‐induced marked QT‐prolongation
Author:
Affiliation:
1. Division of Trauma Emergency Surgery and Surgical Critical CareMassachusetts General HospitalBoston Massachusetts
2. Division of Cardiology, Department of Internal MedicineAmerican University of Beirut Medical CenterBeirut Lebanon
Publisher
Wiley
Subject
Physiology (medical),Cardiology and Cardiovascular Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/jce.14572
Reference15 articles.
1. Cardiac sodium channel mutation associated with epinephrine-induced QT prolongation and sinus node dysfunction
2. Genomic organization and mutational analysis of HERG , a gene responsible for familial long QT syndrome
3. Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias
4. Executive summary: HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes
5. Utility of the Exercise Electrocardiogram Testing in Sudden Cardiac Death Risk Stratification
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