Towards Precision Medicine With Human iPSCs for Cardiac Channelopathies
Abstract
Long-QT syndrome, a frequently fatal inherited arrhythmia syndrome caused by genetic variants (congenital) or drugs (acquired), affects 1 in 2000 people worldwide. Its sentinel event is often sudden cardiac death, which makes preclinical diagnosis by genetic testing potentially life-saving. Unfortunately, clinical experience with genetic testing has shown that it is difficult to correctly identify genetic variants as disease causing. These...
Paper Details
Title
Towards Precision Medicine With Human iPSCs for Cardiac Channelopathies
Published Date
Aug 30, 2019
Journal
Volume
125
Issue
6
Pages
653 - 658
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