Derst, C <br/><br/>
Mutations in the ROMK gene in antenatal Bartter syndrome are associated with impaired K+ channel function.  [electronic resource] 

 -  Biochemical and biophysical research communications  Jan 1997 
 - 641-5 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0006-291X 
<br/><br/><label>Standard No.: </label>10.1006/bbrc.1996.6024  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Animals<br/>Bartter Syndrome--genetics<br/>Child<br/>Child, Preschool<br/>Female<br/>Genes<br/>Humans<br/>Kidney--metabolism<br/>Male<br/>Mutation<br/>Potassium Channels--genetics<br/>Rats<br/>Syndrome