Dias, Alex Marcel Moreira <br/><br/>
Further evidence for loss-of-function mutations in the CEACAM16 gene causing nonsyndromic autosomal recessive hearing loss in humans.  [electronic resource] 

 -  Journal of human genetics  Mar 2019 
 - 257-260 p.  digital 
<br/><br/> Publication Type: Journal Article 
<br/><br/><label>ISSN: </label>1435-232X 
<br/><br/><label>Standard No.: </label>10.1038/s10038-018-0546-4  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Antigens, CD--genetics<br/>Cell Adhesion Molecules--genetics<br/>Deafness--genetics<br/>Female<br/>GPI-Linked Proteins--genetics<br/>Genes, Recessive<br/>Humans<br/>Male<br/>Mutation<br/>Pedigree