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 ✦
P2.04 DMRV and GNE mutations: genotype–phenotype correlation in 100 Japanese patients
✍ Scribed by H. Tomimitsu; A. Arai; K. Murayama; J. Shimizu; N. Suzuki; T. Nagata; M. Aoki; H. Mizusawa; K. Tanaka; I. Nishino
- Book ID
- 116794506
- Publisher
- Elsevier Science
- Year
- 2010
- Tongue
- English
- Weight
- 38 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0960-8966
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