Hashemi, Seyed Basir <br/><br/>
Prevalence of GJB2 (CX26) gene mutations in south Iranian patients with autosomal recessive nonsyndromic sensorineural hearing loss.  [electronic resource] 

 -  Molecular biology reports  Dec 2012 
 - 10481-7 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1573-4978 
<br/><br/><label>Standard No.: </label>10.1007/s11033-012-1929-9  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Connexin 26<br/>Connexins--chemistry<br/>Genes, Recessive--genetics<br/>Genetic Predisposition to Disease<br/>Geography<br/>Hearing Loss, Sensorineural--epidemiology<br/>Humans<br/>Iran--epidemiology<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Mutation Rate<br/>Prevalence<br/>Protein Structure, Tertiary