Andersen-Tawil syndrome (ATS) is a rare inherited disorder characterized by periodic paralysis, mild dysmorphic features, and QT or QU prolongation with ventricular arrhythmias in electrocardiograms (ECGs). Mutations of KCNJ2, encoding the human inward rectifying potassium channel Kir 2.1, have been
✦ LIBER ✦
Mutations ofKCNJ2gene associated with Andersen–Tawil syndrome in Korean families
✍ Scribed by Byung-Ok Choi; Joonki Kim; Bum Chun Suh; Jin Seok Yu; Il Nam Sunwoo; Song Ja Kim; Gwang Hoon Kim; Ki Wha Chung
- Publisher
- Nature Publishing Group
- Year
- 2007
- Tongue
- English
- Weight
- 191 KB
- Volume
- 52
- Category
- Article
- ISSN
- 1435-232X
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