Chen, Q <br/><br/>
Homozygous deletion in KVLQT1 associated with Jervell and Lange-Nielsen syndrome.  [electronic resource] 

 -  Circulation  Mar 1999 
 - 1344-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>0009-7322 
<br/><br/><label>Standard No.: </label>10.1161/01.cir.99.10.1344  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Chromosomes, Human, Pair 11--genetics<br/>DNA Mutational Analysis<br/>Ethnicity--genetics<br/>Female<br/>Frameshift Mutation<br/>Genes, Recessive<br/>Humans<br/>Ion Transport<br/>KCNQ Potassium Channels<br/>KCNQ1 Potassium Channel<br/>Long QT Syndrome--ethnology<br/>Male<br/>Pedigree<br/>Phenotype<br/>Polymorphism, Single-Stranded Conformational<br/>Potassium--metabolism<br/>Potassium Channels--chemistry<br/>Potassium Channels, Voltage-Gated<br/>Sequence Deletion