Kalay, E <br/><br/>
Four novel TMC1 (DFNB7/DFNB11) mutations in Turkish patients with congenital autosomal recessive nonsyndromic hearing loss.  [electronic resource] 

 -  Human mutation  Dec 2005 
 - 591 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1098-1004 
<br/><br/><label>Standard No.: </label>10.1002/humu.9384  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Connexin 26<br/>Connexins--genetics<br/>DNA Mutational Analysis<br/>Female<br/>Frameshift Mutation<br/>Genetic Linkage<br/>Genetic Testing<br/>Haplotypes<br/>Hearing Loss--congenital<br/>Humans<br/>Male<br/>Membrane Proteins--chemistry<br/>Molecular Sequence Data<br/>Mutation, Missense<br/>Pedigree<br/>Sequence Alignment<br/>Turkey