| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8668920 | Journal of Electrocardiology | 2018 | 19 Pages |
Abstract
A pathogenic mutation in RYR2 (p.P164S) is the likely cause of USD in a Chinese family associated with malignant ventricular arrhythmias. Whole exome and target capture sequencing can be useful for discovering the genetic causes of USD.
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Authors
Yubi MD, Siqi He, Zili MD, Ruiling Feng, Ruilin MD, Yongzheng MD, Nan MD, Hang MD, Jia MD, Zifeng MD, Heping MD, Yang MD, Fang MD, Chunyu MD, Yumei MD, Guolin MD, Bin MD, Hua MD, Shulin MD,