alexa Molecular Analysis of <em>KCNQ1, KCNH2</em> and <em>SCN5A</em> Genes in Iranian Patients with Long QT Syndrome | OMICS International| Abstract
ISSN: 1747-0862

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  • Research Article   
  • J Mol Genet Med 2018, Vol 12(3): 359
  • DOI: 10.4172/1747-0862.1000359

Molecular Analysis of KCNQ1, KCNH2 and SCN5A Genes in Iranian Patients with Long QT Syndrome

Amirian A1, Karimipoor M1, Zafari Z1,2, Kallhor M2, Dalili M3*, Saber S3, Fazelifar AF3 and Zeinali S1,4*
1Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, Tehran, Iran
2Department of Medical Genetics, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran
3Cardiac Electrophysiology Research Center, Rajaie Cardiovascular Medical, and Research Center, Iran University of Medical Sciences, Tehran, Iran
4Medical Genetics Laboratory, Kawsar Human Genetics Research Center, Tehran, Iran
*Corresponding Author (s) : Dr. Dalili M, Rajaei, Cardiac Electrophysiology Research Center, Cardiovascular, Medical and Research Center, Vali- Asr Avenue, P.O. Box. 1996911151, Tehran, Iran, Tel: +98-2123922509, Email: [email protected]
Prof. Zeinali S, Department of Molecular Medicine, Biotechnology Research Center, Pasteur Institute of Iran, P.O. Box. 1316943551, Tehran, Iran, Tel: +98-2166969293, Email: [email protected]

Received Date: Aug 10, 2018 / Accepted Date: Aug 21, 2018 / Published Date: Aug 24, 2018

Keywords: Long QT syndrome, Cardiac repolarization, Genetics; De novo mutation, Iran

Citation: Amirian A, Karimipoor M, Zafari Z, Kallhor M, Dalili M, et al. (2018) Molecular Analysis of KCNQ1, KCNH2 and SCN5A Genes in Iranian Patients with Long QT Syndrome. J Mol Genet Med 12: 359 Doi: 10.4172/1747-0862.1000359

Copyright: ©2018 Amirian A, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

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