Li, Tung-Cheng <br/><br/>
Association between mutations in the gap junction β4 gene and nonsyndromic hearing loss: genotype-phenotype correlation patterns.  [electronic resource] 

 -  Molecular medicine reports  Jan 2015 
 - 619-24 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1791-3004 
<br/><br/><label>Standard No.: </label>10.3892/mmr.2014.2725  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Child<br/>Connexins--chemistry<br/>Deafness--diagnosis<br/>Ear, Inner--diagnostic imaging<br/>Genetic Association Studies<br/>Genotype<br/>Hearing Tests<br/>Humans<br/>Mutation<br/>Phenotype<br/>Severity of Illness Index<br/>Temporal Bone--diagnostic imaging<br/>Tomography, X-Ray Computed