A case of long QT syndrome with triple gene abnormalities: Digenic mutations in KCNH2 and SCN5A and gene variant in KCNE1

Published 2012 View Full Article

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Title
A case of long QT syndrome with triple gene abnormalities: Digenic mutations in KCNH2 and SCN5A and gene variant in KCNE1
Authors
Keywords
-
Journal
HEART RHYTHM
Volume 10, Issue 4, Pages 600-603
Publisher
Elsevier BV
Online
2012-12-11
DOI
10.1016/j.hrthm.2012.12.008

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