Prasad, S <br/><br/>
Genetic testing for hereditary hearing loss: connexin 26 (GJB2) allele variants and two novel deafness-causing mutations (R32C and 645-648delTAGA).  [electronic resource] 

 -  Human mutation  Dec 2000 
 - 502-8 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/1098-1004(200012)16:6<502::AID-HUMU7>3.0.CO;2-4  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Alleles<br/>Amino Acid Substitution--genetics<br/>Arginine--genetics<br/>Connexin 26<br/>Connexins--blood<br/>Cysteine--genetics<br/>Deafness--congenital<br/>Genetic Testing--methods<br/>Genetic Variation<br/>Hearing Loss, Sensorineural--congenital<br/>Humans<br/>Mutation--genetics<br/>Sequence Deletion--genetics