Casimiro, M C <br/><br/>
Targeted disruption of the Kcnq1 gene produces a mouse model of Jervell and Lange-Nielsen Syndrome.  [electronic resource] 

 -  Proceedings of the National Academy of Sciences of the United States of America  Feb 2001 
 - 2526-31 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0027-8424 
<br/><br/><label>Standard No.: </label>10.1073/pnas.041398998  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Action Potentials<br/>Animals<br/>Base Sequence<br/>DNA Primers<br/>Disease Models, Animal<br/>Ear, Inner--metabolism<br/>Electrocardiography<br/>Homeostasis--genetics<br/>KCNQ Potassium Channels<br/>KCNQ1 Potassium Channel<br/>Long QT Syndrome--genetics<br/>Mice<br/>Mice, Mutant Strains<br/>Mutation<br/>Phenotype<br/>Potassium Channels--genetics<br/>Potassium Channels, Voltage-Gated