Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: Evidence for clinically significant IKr-IKs α-subunit interaction

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Title
Trafficking-deficient long QT syndrome mutation KCNQ1-T587M confers severe clinical phenotype by impairment of KCNH2 membrane localization: Evidence for clinically significant IKr-IKs α-subunit interaction
Authors
Keywords
-
Journal
HEART RHYTHM
Volume 6, Issue 12, Pages 1792-1801
Publisher
Elsevier BV
Online
2009-08-14
DOI
10.1016/j.hrthm.2009.08.009

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