The Phenotype Characteristics of Type-13 Long QT Syndrome with mutation in KCNJ5 (Kir3.4-G387R)
Research output: Contribution to journal › Journal article › peer-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 language | English |
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Journal | Heart rhythm : the official journal of the Heart Rhythm Society |
Volume | 10 |
Issue number | 10 |
Pages (from-to) | 1500-1506 |
Number of pages | 7 |
ISSN | 1547-5271 |
DOIs | |
Publication status | Published - Oct 2013 |
ID: 48051903