Interpreting Incidentally Identified Variants in Genes Associated with Catecholaminergic Polymorphic Ventricular Tachycardia in a Large Cohort of Clinical Whole Exome Genetic Test Referrals

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 fo...

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Publicado no:Circ Arrhythm Electrophysiol
Main Authors: 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.
Formato: Artigo
Idioma:Inglês
Publicado em: 2017
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5391872/
https://ncbi.nlm.nih.gov/pubmed/28404607
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1161/CIRCEP.116.004742
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