Faridi, R <br/><br/>
Mutations of SGO2 and CLDN14 collectively cause coincidental Perrault syndrome.  [electronic resource] 

 -  Clinical genetics  02 2017 
 - 328-332 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/cge.12867  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Cell Cycle Proteins--genetics<br/>Claudins--genetics<br/>Consanguinity<br/>Exome--genetics<br/>Female<br/>Gonadal Dysgenesis, 46,XX--genetics<br/>Hearing Loss, Sensorineural--genetics<br/>Homozygote<br/>Humans<br/>Male<br/>Mice<br/>Mutation<br/>Pedigree