Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole‐exome sequencing

Identification of a novel pathogenic variant in KCNH2 in an Iranian family with long QT syndrome 2 by whole‐exome sequencing

Abstract Background Long QT syndrome (LQTS) is a lethal cardiac condition. However, the clinical implementation of genetic testing has now made LQTS eminently treatable. Next‐generation sequencing has remarkable potential for both clinical diagnostics and research of LQTS. Here, we investigated the...

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Bibliographic Details
Main Authors: Amir Farjam Fazelifar, Maryam Pourirahim, Tannaz Masoumi, Alireza Biglari, Majid Maleki, Samira Kalayinia
Format: Article
Language:English
Published: Wiley 2023-06-01
Series:Journal of Arrhythmia
Subjects:
KCNH2 gene
long QT syndrome
variant
whole‐exome sequencing
Online Access:https://doi.org/10.1002/joa3.12857

Internet

https://doi.org/10.1002/joa3.12857

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