PMID 25589040 2015 Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.
rs876661405 in
LOC107985305;CEACAM16 gene and
DEAFNESS, AUTOSOMAL DOMINANT 4B
PMID 25589040 2015 Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.
PMID 21368133 2011 Carcinoembryonic antigen-related cell adhesion molecule 16 interacts with alpha-tectorin and is mutated in autosomal dominant hearing loss (DFNA4).