TY  - GEN
AU  - Muñoz-Esparza,Carmen
AU  - García-Molina,Esperanza
AU  - Salar-Alcaraz,Mariela
AU  - Peñafiel-Verdú,Pablo
AU  - Sánchez-Muñoz,Juan J
AU  - Martínez Sánchez,Juan
AU  - Cabañas-Perianes,Valentín
AU  - Valdés Chávarri,Mariano
AU  - García Alberola,Arcadio
AU  - Gimeno-Blanes,Juan R
TI  - Heterogeneous Phenotype of Long QT Syndrome Caused by the KCNH2-H562R Mutation: Importance of Familial Genetic Testing
SN  - 1885-5857
PY  - 2016///1213
KW  - Aged
KW  - Aged, 80 and over
KW  - Child, Preschool
KW  - DNA
KW  - genetics
KW  - DNA Mutational Analysis
KW  - ERG1 Potassium Channel
KW  - Electrocardiography
KW  - Female
KW  - Genetic Testing
KW  - Heart Conduction System
KW  - physiopathology
KW  - Heterozygote
KW  - Humans
KW  - Long QT Syndrome
KW  - Male
KW  - Mutation
KW  - Pedigree
KW  - Phenotype
KW  - Young Adult
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1016/j.rec.2014.10.022
ER  -