𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Cardiac conduction defects associate with mutations in SCN5A

✍ Scribed by Schott, Jean-Jacques; Alshinawi, Connie; Kyndt, Florence; Probst, Vincent; Hoorntje, Theo M.; Hulsbeek, Miriam; Wilde, Arthur A.M.; Escande, Denis; Mannens, Marcel M.A.M.; Le Marec, Hervé


Book ID
109494132
Publisher
Nature Publishing Group
Year
1999
Tongue
English
Weight
216 KB
Volume
23
Category
Article
ISSN
1061-4036

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


A homozygous SCN5A mutation in a severe,
✍ Axel Neu; Michele Eiselt; Matthias Paul; Kathrin Sauter; Birgit Stallmeyer; Dirk 📂 Article 📅 2010 🏛 John Wiley and Sons 🌐 English ⚖ 460 KB

Cardiac sodium channels are key players in the generation and propagation of action potentials in the human heart. Heterozygous mutations in the SCN5A gene have been found to be associated with long QT syndrome, Brugada syndrome, and sinus node dysfunction (SND). Recently, overlapping arrhythmia phe

Identification of a new SCN5A mutation,
✍ Jesaia Benhorin; Maya Goldmit; Jean W. MacCluer; John Blangero; Ruth Goffen; Aye 📂 Article 📅 1998 🏛 John Wiley and Sons 🌐 English ⚖ 61 KB

The long QT syndrome (LQT) is an inherited cardiac disorder that can cause sudden cardiac death among apparently healthy young individuals due to malignant ventricular arrhythmias. LQT was found to be caused by mutations in four genes LQT1, LQT2, LQT3 and LQT5, and linkage was reported for an additi