An InterdomainKCNH2Mutation Produces an Intermediate Long QT Syndrome

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Lack of association between coding region of KCNE2 gene and the congenital long QT syndrome in an Iranian population

Introduction: Congenital long QT syndrome (LQTS) is a cardiac disorder characterized by QT interval prolongation at basal ECG. Different LQTS genes encode ion channel subunits or proteins involved in regulating cardiac ionic currents. Long QT syndrome type 6 (LQT6) is caused by mutation in the KCNE2 gene. Our research aimed to analyze genetic variants of KCNE2 gene causing the disease in Irania...

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ژورنال

عنوان ژورنال: Human Mutation

سال: 2015

ISSN: 1059-7794

DOI: 10.1002/humu.22805