Wattanasirichaigoon, D <br/><br/>
High prevalence of V37I genetic variant in the connexin-26 (GJB2) gene among non-syndromic hearing-impaired and control Thai individuals.  [electronic resource] 

 -  Clinical genetics  Nov 2004 
 - 452-60 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>0009-9163 
<br/><br/><label>Standard No.: </label>10.1111/j.1399-0004.2004.00325.x  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Amino Acid Substitution--genetics<br/>Asian People--genetics<br/>Child<br/>Child, Preschool<br/>Connexin 26<br/>Connexins--genetics<br/>Female<br/>Hearing Loss, Sensorineural--ethnology<br/>Humans<br/>Infant<br/>Isoleucine--genetics<br/>Male<br/>Mutation, Missense--genetics<br/>Prevalence<br/>Thailand<br/>Valine--genetics