Loh, Nellie Y <br/><br/>
Autosomal dominant hypercalciuria in a mouse model due to a mutation of the epithelial calcium channel, TRPV5.  [electronic resource] 

 -  PloS one  2013 
 - e55412 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0055412  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Base Sequence<br/>Calbindins<br/>Calcium Channels--genetics<br/>Chromosome Mapping<br/>Genes, Dominant--genetics<br/>Genetic Predisposition to Disease--genetics<br/>Hypercalciuria--genetics<br/>Immunohistochemistry<br/>Mice<br/>Molecular Sequence Data<br/>Mutation, Missense--genetics<br/>Phenotype<br/>S100 Calcium Binding Protein G--metabolism<br/>Sequence Analysis, DNA<br/>TRPV Cation Channels--genetics