Najmabadi, Hossein <br/><br/>
GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss.  [electronic resource] 

 -  Human mutation  May 2002 
 - 572 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S. 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.9033  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Connexin 26<br/>Connexins--genetics<br/>Genes, Recessive--genetics<br/>Genetic Carrier Screening--methods<br/>Genetic Testing--methods<br/>Hearing Disorders--genetics<br/>Humans<br/>Iran--epidemiology<br/>Mutation--genetics<br/>Syndrome