Cengiz, Filiz Basak <br/><br/>
Novel pathogenic variants underlie SLC26A4-related hearing loss in a multiethnic cohort.  [electronic resource] 

 -  International journal of pediatric otorhinolaryngology  Oct 2017 
 - 167-171 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1872-8464 
<br/><br/><label>Standard No.: </label>10.1016/j.ijporl.2017.08.006  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Ear, Inner--pathology<br/>Female<br/>Hearing Loss, Sensorineural--genetics<br/>Humans<br/>Iran<br/>Male<br/>Membrane Transport Proteins--genetics<br/>Mexico<br/>Mutation<br/>Sequence Analysis, DNA<br/>Sulfate Transporters<br/>Turkey