A novel SCN5A mutation associated with long QT-3: altered inactivation kinetics and channel dysfunction. [electronic resource]
- Physiological genomics Sep 2002
- 191-7 p. digital
Publication Type: Case Reports; Journal Article; Research Support, U.S. Gov't, P.H.S.
1531-2267
10.1152/physiolgenomics.00039.2002 doi
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