A novel SCN5A mutation associated with long QT-3: altered inactivation kinetics and channel dysfunction. [electronic resource]
Producer: 20021115Description: 191-7 p. digitalISSN:- 1531-2267
- Adolescent
- Cell Line
- DNA -- chemistry
- DNA Mutational Analysis
- Genotype
- Humans
- Kinetics
- Long QT Syndrome -- complications
- Male
- Membrane Potentials -- drug effects
- Mutation
- NAV1.5 Voltage-Gated Sodium Channel
- Patch-Clamp Techniques
- Plasmids -- genetics
- Sodium Channels -- genetics
- Syncope -- etiology
- Tachycardia, Ventricular -- etiology
- Tetrodotoxin -- pharmacology
- Transfection
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Publication Type: Case Reports; Journal Article; Research Support, U.S. Gov't, P.H.S.
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