Vahid Khori

Ischemic Disorders Research Center, Golestan University of Medical Sciences, Gorgan, Iran

[ 1 ] - 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...

نویسندگان همکار

Ayyoob Khosravi 1  

Majid Haghjoo 1  

Mehdi Gholizadeh 1  

Mehdi Zahedi 1  

Morteza Oladnabi 1  

Pedram Torabian 1  

Yahya Jand 1