Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole-exome sequencing.
Amir Farjam FazelifarMaryam PourirahimTannaz MasoumiAlireza BiglariMajid MalekiSamira KalayiniaPublished in: Journal of arrhythmia (2023)
screening in a pedigree with SCD cases.