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

Biochemical and Biophysical Research Communications 2010 Vol. 395; Iss. 1

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

Alessandro Terrinoni, Andrea Codispoti, Valeria Serra, Ernesto Bruno, Biagio Didona, Mauro Paradisi, Steven Nisticò, Elena Campione, Bianca Napolitano, Laura Diluvio, Gerry Melino
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Volume:
395
Year:
2010
Language:
english
Pages:
31
DOI:
10.1016/j.bbrc.2010.03.098
File:
PDF, 602 KB
english, 2010
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