Jongbloed, Roselie <br/><br/>
DHPLC analysis of potassium ion channel genes in congenital long QT syndrome.  [electronic resource] 

 -  Human mutation  Nov 2002 
 - 382-91 p.  digital 
<br/><br/> Publication Type: Evaluation Study; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.10131  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Cation Transport Proteins<br/>Chromatography, High Pressure Liquid--methods<br/>DNA Mutational Analysis--methods<br/>Ether-A-Go-Go Potassium Channels<br/>KCNQ Potassium Channels<br/>KCNQ1 Potassium Channel<br/>Long QT Syndrome--genetics<br/>Molecular Sequence Data<br/>Mutation<br/>Nucleic Acid Denaturation<br/>Polymerase Chain Reaction<br/>Polymorphism, Single Nucleotide<br/>Potassium Channels--genetics<br/>Potassium Channels, Voltage-Gated