Сhurbanov, Alexander Y <br/><br/>
Whole Exome Sequencing Reveals Homozygous Mutations in RAI1, OTOF, and SLC26A4 Genes Associated with Nonsyndromic Hearing Loss in Altaian Families (South Siberia).  [electronic resource] 

 -  PloS one  2016 
 - e0153841 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0153841  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Cohort Studies<br/>DNA Mutational Analysis<br/>Deafness--genetics<br/>Exome<br/>Exons<br/>Family Health<br/>Female<br/>Genetic Variation<br/>Genome, Human<br/>Geography<br/>Homozygote<br/>Humans<br/>Male<br/>Membrane Proteins--genetics<br/>Membrane Transport Proteins--genetics<br/>Mutation<br/>Mutation, Missense<br/>Pedigree<br/>Siberia<br/>Sulfate Transporters<br/>Trans-Activators<br/>Transcription Factors--genetics