A novel KCNH2 frameshift mutation (c.46delG) associated with high risk of sudden death in a family with congenital long QT syndrome type 2
Yoo, Hyun Sok, Medina, Nancy, von Wulffen, María Alejandra, Ciampi, Natalia, Paolucci, Analia, Garro, Hugo Ariel, Principato, Mario Bruno, Acunzo, Rafael Salvador, Carbajales, Justo
Published in International journal of arrhythmia (01.01.2021)
Published in International journal of arrhythmia (01.01.2021)
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