Anwar, Saima <br/><br/>
SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis.  [electronic resource] 

 -  Journal of human genetics  May 2009 
 - 266-70 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Intramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1435-232X 
<br/><br/><label>Standard No.: </label>10.1038/jhg.2009.21  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Abnormalities, Multiple--genetics<br/>Amino Acid Sequence<br/>Case-Control Studies<br/>Chromosomes, Human, Pair 7--genetics<br/>Deafness--complications<br/>Exons--genetics<br/>Genetic Predisposition to Disease<br/>Haplotypes--genetics<br/>Homozygote<br/>Humans<br/>Membrane Transport Proteins--chemistry<br/>Microsatellite Repeats--genetics<br/>Molecular Sequence Data<br/>Mutation--genetics<br/>Pakistan--ethnology<br/>Physical Chromosome Mapping<br/>Polymorphism, Single Nucleotide--genetics<br/>Sequence Alignment<br/>Sulfate Transporters<br/>Syndrome