Zhang, Q-J <br/><br/>
High frequency of OTOF mutations in Chinese infants with congenital auditory neuropathy spectrum disorder.  [electronic resource] 

 -  Clinical genetics  09 2016 
 - 238-46 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/cge.12744  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Audiometry<br/>Child<br/>Child, Preschool<br/>China<br/>Female<br/>Genetic Predisposition to Disease<br/>Hearing Disorders--diagnosis<br/>Hearing Loss, Central--diagnosis<br/>Humans<br/>Infant<br/>Male<br/>Membrane Proteins--genetics<br/>Mutation