Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2
- 1 February 2000
- journal article
- case report
- Published by Wiley in Clinical Genetics
- Vol. 57 (2) , 125-130
Abstract
In a four‐generation family with long QT syndrome, syncopes and torsades de pointes ventricular tachycardia (TdP) were elicited by abrupt awakening in the early morning hours. The syndrome was associ...Keywords
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