Associated Papers
Fetal Arrhythmia Leading to a Diagnosis of Congenital Long QT Syndrome Type II.
Milner A et al.
Jacc. Case Reports, 2024
Case Report: Prenatal Whole-Exome Sequencing Identified a Novel Nonsense Mutation of the KCNH2 Gene in a Fetus With Familial 2q14.2 Duplication.
Zhuang J et al.
Frontiers in Genetics, 2022
Implantable cardioverter defibrillator therapy in repaired tetralogy of Fallot after pulmonary valve replacement: Implications for the mechanism of ventricular arrhythmia.
Chiu SN et al.
International Journal of Cardiology, 2017
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