The Phenotype Characteristics of Type-13 Long QT Syndrome with mutation in KCNJ5 (Kir3.4-G387R)

Research output: Contribution to journalJournal articleResearchpeer-review

Long QT syndrome type 13 (LQT13) is caused by loss-of-function mutation in the KCNJ5-encoded cardiac G-protein coupled inward rectifier potassium channel Kir3.4. The electrocardiographic (ECG) features of LQT13 are not described yet.
Original languageEnglish
JournalHeart rhythm : the official journal of the Heart Rhythm Society
Issue number10
Pages (from-to)1500-1506
Number of pages7
Publication statusPublished - Oct 2013

ID: 48051903