Referenced in: none

Automatically associated channels: Kv11.1

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

Authors: Carmen Muñoz-Esparza, Esperanza García-Molina, Mariela Salar-Alcaraz, Pablo Peñafiel-Verdú, Juan J Sánchez-Muñoz, Juan Martínez Sánchez, Valentín Cabañas-Perianes, Mariano Valdés Chávarri, Arcadio García Alberola, Juan R Gimeno-Blanes

Journal, date & volume: Rev Esp Cardiol (Engl Ed), 2015 Mar 25 , ,

PubMed link: http://www.ncbi.nlm.nih.gov/pubmed/25819988

Abstract