Combination of cardiac conduction disease and long QT syndrome caused by mutation T1620K in the cardiac sodium channel. [electronic resource]
Producer: 20080829Description: 740-8 p. digitalISSN:- 0008-6363
- Action Potentials
- Adolescent
- Adult
- Ajmaline -- therapeutic use
- Animals
- Anti-Arrhythmia Agents -- therapeutic use
- Bundle-Branch Block -- drug therapy
- Cell Line
- Child
- DNA Mutational Analysis
- Death, Sudden, Cardiac -- etiology
- Electrocardiography
- Female
- Gene Transfer Techniques
- Genetic Predisposition to Disease
- Humans
- Kinetics
- Lidocaine -- therapeutic use
- Long QT Syndrome -- drug therapy
- Lysine
- Male
- Muscle Proteins -- drug effects
- Mutation
- Myocardium -- metabolism
- NAV1.5 Voltage-Gated Sodium Channel
- Patch-Clamp Techniques
- Pedigree
- Sodium -- metabolism
- Sodium Channels -- drug effects
- Syncope -- genetics
- Threonine
- Xenopus laevis
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.