Detection of Variants in Patients with Idiopathic Ventricular Fibrillation by Whole-exome Sequencing.

Aims And Background: Idiopathic ventricular fibrillation (IVF) is a cause of sudden cardiac death (SCD). The frequency of mutations in disease-causing genes ranges, on average, between 16 and 48% in SCD cases. This study aimed to identify novel mutations in IVF patients without , and mutations using whole-exome sequencing (WES).