A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitation
Abstract PRKAG2 syndrome is a rare autosomal dominant inherited disorder that is characterized by cardiac hypertrophy, ventricular pre-excitation and conduction system abnormalities. There is little knowledge in cardiovascular magnetic resonance (CMR) characteristics of PRKAG2 cardiomyopathy. This s...
Saved in:
| Main Authors: | , , , , , , , , , , , , |
|---|---|
| Format: | article |
| Language: | EN |
| Published: |
Nature Portfolio
2017
|
| Subjects: | |
| Online Access: | https://doaj.org/article/5acc6955e994498e811bcbc02fa0346f |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|