Gao, Xue <br/><br/>
Novel compound heterozygous TMC1 mutations associated with autosomal recessive hearing loss in a Chinese family.  [electronic resource] 

 -  PloS one  2013 
 - e63026 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0063026  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Amino Acid Sequence<br/>Animals<br/>Asian People--genetics<br/>Base Sequence<br/>DNA Mutational Analysis<br/>Exome--genetics<br/>Female<br/>Hearing Loss, Sensorineural--genetics<br/>Heterozygote<br/>Humans<br/>Male<br/>Membrane Proteins--chemistry<br/>Mice<br/>Molecular Sequence Data<br/>Pedigree<br/>Polymorphism, Genetic<br/>Rats<br/>Siblings<br/>Young Adult