Molecular Approach of Hereditary Arrhythmias, Long QT Syndrome, and Arrhythmogenic Right Ventricular Cardiomyopathy

Background: Hereditary cardiac arrhythmias result from mutations in various genes encoding ion channels. One major channelopathy is long QT syndrome, which has excel-lent genetic and clinical heterogeneity. Arrhythmogenic right ventricular cardiomyopathy, another hereditary arrhythmia type, also sho...

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Bibliographic Details
Main Authors: Hanife Saat, Ibrahim Şahin, Haktan Bagğış Erdem, Senem Özgür, Semiha Terlemez Tokgöz, Taha Bahsi&775;
Format: Article
Language:English
Published: KARE Publishing 2022-06-01
Series:Anatolian Journal of Cardiology
Subjects:
Online Access:https://jag.journalagent.com/z4/download_fulltext.asp?pdir=anatoljcardiol&un=AJC-96800