Jörs, Simone <br/><br/>
Genetic inactivation of Trpml3 does not lead to hearing and vestibular impairment in mice.  [electronic resource] 

 -  PloS one  Dec 2010 
 - e14317 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0014317  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Brain Stem--physiology<br/>Cations<br/>Cell Line<br/>Cytosol--metabolism<br/>Exons<br/>Gene Deletion<br/>Genotype<br/>Hearing--genetics<br/>Hearing Loss--genetics<br/>Humans<br/>Hydrogen--chemistry<br/>Mice<br/>Mice, Knockout<br/>Models, Genetic<br/>Mutation<br/>Phenotype<br/>Protein Isoforms<br/>Sodium--chemistry<br/>TRPM Cation Channels--genetics<br/>Transient Receptor Potential Channels<br/>Vestibular Diseases--genetics