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

Publikation: Bidrag til tidsskriftTidsskriftartikelfagfællebedømt

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.
OriginalsprogEngelsk
TidsskriftHeart rhythm : the official journal of the Heart Rhythm Society
Vol/bind10
Udgave nummer10
Sider (fra-til)1500-1506
Antal sider7
ISSN1547-5271
DOI
StatusUdgivet - okt. 2013

ID: 48051903