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    A novel KCNH2 frameshift mutation (c.46delG) associated with high risk of sudden death in a family with congenital long QT syndrome type 2

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


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