Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing
- 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.
ISSN: 1579-2242, 0300-8932
Argitalpen urtea: 2015
Alea: 68
Zenbakia: 10
Orrialdeak: 861-868
Mota: Artikulua