Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutation

Published 2012 View Full Article

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Title
Genetic variants in SCN5A promoter are associated with arrhythmia phenotype severity in patients with heterozygous loss-of-function mutation
Authors
Keywords
-
Journal
HEART RHYTHM
Volume 9, Issue 7, Pages 1090-1096
Publisher
Elsevier BV
Online
2012-02-25
DOI
10.1016/j.hrthm.2012.02.023

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