𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Is enhanced inward rectification of KCNJ2 in Andersen–Tawil syndrome is arrhythmogenic phenotype?

✍ Scribed by Yoshinori Tani; Daiji Miura; Kazufumi Nakamura; Junko Kurokawa; Tohru Ohe; Tetsushi Furukawa


Book ID
116984463
Publisher
Elsevier Science
Year
2006
Tongue
English
Weight
55 KB
Volume
41
Category
Article
ISSN
0022-2828

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Genotype-phenotype correlations of KCNJ2
✍ Yoshisumi Haruna; Atsushi Kobori; Takeru Makiyama; Hidetada Yoshida; Masaharu Ak 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 455 KB

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