Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome

Volume: 15, Issue: 1
Published: Apr 20, 2017
Abstract
Hypertrophic cardiomyopathy (HCM) patients with early repolarization (ER) pattern are at higher risk of ventricular arrhythmia, yet the genetic background of this situation has not been well investigated. Here we report novel trigenic mutations detected in a Chinese family of obstructive HCM with ER and short QT syndrome (SQTS).Proband and family members underwent detailed medical assessments. DNAs were extracted from peripheral blood leukocytes...
Paper Details
Title
Novel trigenic CACNA1C/DES/MYPN mutations in a family of hypertrophic cardiomyopathy with early repolarization and short QT syndrome
Published Date
Apr 20, 2017
Volume
15
Issue
1
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