Wang, D W <br/><br/>
Characterization of human cardiac Na+ channel mutations in the congenital long QT syndrome.  [electronic resource] 

 -  Proceedings of the National Academy of Sciences of the United States of America  Nov 1996 
 - 13200-5 p.  digital 
<br/><br/> Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0027-8424 
<br/><br/><label>Standard No.: </label>10.1073/pnas.93.23.13200  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Base Sequence<br/>Cell Line<br/>Cloning, Molecular<br/>DNA Primers<br/>Heart--physiology<br/>Humans<br/>Kidney<br/>Kinetics<br/>Long QT Syndrome--genetics<br/>Mammals<br/>Membrane Potentials<br/>Muscular Diseases--physiopathology<br/>Mutagenesis, Site-Directed<br/>NAV1.5 Voltage-Gated Sodium Channel<br/>Oligodeoxyribonucleotides<br/>Patch-Clamp Techniques<br/>Point Mutation<br/>Polymerase Chain Reaction<br/>Recombinant Proteins--biosynthesis<br/>Sodium Channels--genetics<br/>Transfection