Installation

Journal of cardiology
Authors
Abstract

The development of candidate gene approaches to enable molecular diagnosis of hypertrophic cardiomyopathy (HCM) has required extensive and prolonged efforts. Whole exome sequencing (WES) technologies have already accelerated genetic studies of Mendelian disorders, yielding approximately 30% diagnostic success. As a result, there is great interest in extending the use of WES to any of Mendelian diseases. This study investigated the potential of WES for molecular diagnosis of HCM.

Year of Publication
2015
Journal
Journal of cardiology
Date Published
2015/10/03
ISSN
0914-5087
URL
DOI
10.1016/j.jjcc.2015.09.003
Links