Pingault, Veronique <br/><br/>
Loss-of-function mutations in SOX10 cause Kallmann syndrome with deafness.  [electronic resource] 

 -  American journal of human genetics  May 2013 
 - 707-24 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1537-6605 
<br/><br/><label>Standard No.: </label>10.1016/j.ajhg.2013.03.024  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>DNA Mutational Analysis<br/>Deafness--genetics<br/>Female<br/>France<br/>Galactosides<br/>Genetic Predisposition to Disease--genetics<br/>HeLa Cells<br/>Humans<br/>Indoles<br/>Kallmann Syndrome--genetics<br/>Male<br/>Mice<br/>Mutation--genetics<br/>Neuroglia--pathology<br/>Olfactory Pathways--pathology<br/>Plasmids--genetics<br/>SOXE Transcription Factors--genetics