Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing

1. Muñoz-Esparza, C.
2. García-Molina, E.
3. Salar-Alcaraz, M.
4. Peñafiel-Verdú, P.
5. Sánchez-Muñoz, J.J.
6. Martínez Sánchez, J.
7. Cabañas-Perianes, V.
8. Valdés Chávarri, M.
9. García Alberola, A.
10. Gimeno-Blanes, J.R.