The Phenotype Characteristics of Type-13 Long QT Syndrome with mutation in KCNJ5 (Kir3.4-G387R)
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › fagfællebedømt
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.
Originalsprog | Engelsk |
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Tidsskrift | Heart rhythm : the official journal of the Heart Rhythm Society |
Vol/bind | 10 |
Udgave nummer | 10 |
Sider (fra-til) | 1500-1506 |
Antal sider | 7 |
ISSN | 1547-5271 |
DOI | |
Status | Udgivet - okt. 2013 |
ID: 48051903