검색결과 : 2건
| No. | Article |
|---|---|
| 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 |
| 2 |
Denaturing HPLC-based approach for detection of COL7A1 gene mutations causing dystrophic epidermolysis bullosa Posteraro P, Pascucci M, Colombi M, Barlati S, Giannetti A, Paradisi M, Mustonen A, Zambruno G, Castiglia D Biochemical and Biophysical Research Communications, 338(3), 1391, 2005 |