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JHG.2014.114
JHG.2014.114
http://dx.doi.org/10.1038/JHG.2014.114
Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family
P356
Q24314717-2DBE9FB3-0D06-49EF-9DAE-8F2B54AEF41A
P356
JHG.2014.114
http://dx.doi.org/10.1038/JHG.2014.114