Article
Interpreting Incidentally Identified Variants in Genes Associated With Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole-Exome Genetic Test Referrals.
Circulation. Arrhythmia and electrophysiology - 1 Apr 2017
Landstrom Andrew P, Dailey-Schwartz Andrew L, Rosenfeld Jill A, Yang Yaping, McLean Margaret J, Miyake Christina Y, Valdes Santiago O, Fan Yuxin, Allen Hugh D, Penny Daniel J, Kim Jeffrey J
Abstract excerpt
BACKGROUND: The rapid expansion of genetic testing has led to increased utilization of clinical whole-exome sequencing (WES). Clinicians and genetic researchers are being faced with assessing risk of disease vulnerability from incidentally identified genetic variants which is typified by variants found in genes associated with sudden death-predisposing catecholaminergic polymorphic ventricular tachycardia (CPVT)....
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