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Munoz-Esparza, C., García-Molina, E., Salar-Alcaraz, M., Penafiel-Verdú, P., Sánchez-Munoz, J.J., Martínez Sánchez, J., Cabanas-Perianes, V., Valdés Chávarri, M., García Alberola, A. and Gimeno-Blanes, J.R. (2015) Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing. Revista Espanola de Cardiología, 68, 861-868.
https://doi.org/10.1016/j.rec.2014.10.022

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