Rhodes, Charlotte R <br/><br/>
The homeobox gene Emx2 underlies middle ear and inner ear defects in the deaf mouse mutant pardon.  [electronic resource] 

 -  Journal of neurocytology  Nov 2003 
 - 1143-54 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0300-4864 
<br/><br/><label>Standard No.: </label>10.1023/B:NEUR.0000021908.98337.91  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Action Potentials--genetics<br/>Animals<br/>Auditory Threshold--physiology<br/>Cochlea--abnormalities<br/>Ear Ossicles--abnormalities<br/>Ear, Middle--abnormalities<br/>Female<br/>Gene Expression Regulation, Developmental--genetics<br/>Hair Cells, Auditory, Outer--abnormalities<br/>Hearing Loss, Conductive--genetics<br/>Hearing Loss, Sensorineural--genetics<br/>Homeodomain Proteins--genetics<br/>Male<br/>Mice<br/>Mice, Inbred BALB C<br/>Mice, Inbred C3H<br/>Mice, Mutant Strains<br/>Microscopy, Electron, Scanning<br/>Molecular Sequence Data<br/>Mutation, Missense--genetics<br/>Sequence Homology, Amino Acid<br/>Transcription Factors