International Journal of Arrhythmia is affiliated with the Korean Heart Rhythm Society.
A novel KCNH2 frameshift mutation (c.46delG) associated with high risk of sudden death in a family with congenital long QT syndrome type 2
The congenital long QT syndrome type 2 is caused by mutations in KCNH2 gene that encodes the alpha subunit of potassium channel Kv11.1. The carriers of the pathogenic variant of KCNH2 gene manifest a phenotype...
Citation: International Journal of Arrhythmia 2021 22:1