𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Novel mutation (H402R) in the S1 domain of KCNH2-encoded gene associated with long QT syndrome in a Spanish family

✍ Scribed by José J. Zamorano-León; Sergio Alonso-Orgaz; Javier Moreno; Rafael Cinza; Maria J. García-Torrent; Nicasio Pérez-Castellano; Julián Pérez-Villacastín; Carlos Macaya; Antonio J. López-Farré


Book ID
116547683
Publisher
Elsevier Science
Year
2010
Tongue
English
Weight
137 KB
Volume
142
Category
Article
ISSN
0167-5273

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Analysis of the human KCNH2(HERG) gene:
✍ Aimée Paulussen; Ping Yang; Menelas Pangalos; Peter Verhasselt; Roger Marrannes; 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 30 KB 👁 2 views

Long QT (LQT) syndrome is a potentially life-threatening disorder, characterized by a distinct cardiac arrhythmia known as torsades de pointes. Mutations within a number of genes linked to the familial form, including that coding for a cardiac potassium channel called KCNH2 (HERG), have been describ