APA

Muñoz-Esparza C., García-Molina E., Salar-Alcaraz M., Peñafiel-Verdú P., Sánchez-Muñoz J. J., Martínez Sánchez J., Cabañas-Perianes V., Valdés Chávarri M., García Alberola A. & Gimeno-Blanes J. R. (20161213). Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing. : Revista espanola de cardiologia (English ed.).

Chicago

Muñoz-Esparza Carmen, García-Molina Esperanza, Salar-Alcaraz Mariela, Peñafiel-Verdú Pablo, Sánchez-Muñoz Juan J, Martínez Sánchez Juan, Cabañas-Perianes Valentín, Valdés Chávarri Mariano, García Alberola Arcadio and Gimeno-Blanes Juan R. 20161213. Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing. : Revista espanola de cardiologia (English ed.).

Harvard

Muñoz-Esparza C., García-Molina E., Salar-Alcaraz M., Peñafiel-Verdú P., Sánchez-Muñoz J. J., Martínez Sánchez J., Cabañas-Perianes V., Valdés Chávarri M., García Alberola A. and Gimeno-Blanes J. R. (20161213). Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing. : Revista espanola de cardiologia (English ed.).

MLA

Muñoz-Esparza Carmen, García-Molina Esperanza, Salar-Alcaraz Mariela, Peñafiel-Verdú Pablo, Sánchez-Muñoz Juan J, Martínez Sánchez Juan, Cabañas-Perianes Valentín, Valdés Chávarri Mariano, García Alberola Arcadio and Gimeno-Blanes Juan R. Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing. : Revista espanola de cardiologia (English ed.). 20161213.