Simon, D B <br/><br/>
Genetic heterogeneity of Bartter's syndrome revealed by mutations in the K+ channel, ROMK.  [electronic resource] 

 -  Nature genetics  Oct 1996 
 - 152-6 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>1061-4036 
<br/><br/><label>Standard No.: </label>10.1038/ng1096-152  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Bartter Syndrome--genetics<br/>Carrier Proteins--genetics<br/>Cell Membrane--chemistry<br/>Consanguinity<br/>Conserved Sequence<br/>DNA Mutational Analysis<br/>Female<br/>Genetic Heterogeneity<br/>Genotype<br/>Humans<br/>Male<br/>Mutation<br/>Pedigree<br/>Polymorphism, Single-Stranded Conformational<br/>Potassium Channels--chemistry<br/>Potassium Channels, Inwardly Rectifying<br/>Sodium-Potassium-Chloride Symporters