Connexin 26 (GJB2) mutations as a cause of the KID syndrome with hearing loss.

Source:http://linkedlifedata.com/resource/pubmed/id/20307501

Biochem. Biophys. Res. Commun. 2010 Apr 23 395 1 25-30

Download in:

View as

Triples

General Info

PMID
20307501