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2015•Revista Española de Cardiología (English Edition)Requires access

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

Carmen Muñoz‐Esparza, Esperanza García-Molina, Mariela Salar-Alcaraz, Pablo Peñafiel-Verdú, Juan-José Sánchez-Muñoz, Juan Martínez Sánchez, Valentín Cabañas‐Perianes, Mariano Valdés Chávarri, Arcadio García Alberola, Juan R. Gimeno

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Key concepts: Long QT syndrome, Medicine, hERG, Sudden death, QT interval, Sudden cardiac death, Short QT syndrome, Genetic testing

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Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing — Research Paper | ScholarLens