검색결과 : 1건
No. | Article |
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1 |
Connexin 26 (GJB2) mutations as a cause of the KID syndrome with hearing loss Terrinoni A, Codispoti A, Serra V, Bruno E, Didona B, Paradisi M, Nistico S, Campione E, Napolitano B, Diluvio L, Melino G Biochemical and Biophysical Research Communications, 395(1), 25, 2010 |