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Functional characterization of a novel Cx26 (T55N) mutation associated to non-syndromic hearing loss

✍ Scribed by Salvatore Melchionda; Massimiliano Bicego; Elio Marciano; Annamaria Franzè; Marcello Morgutti; Grazia Bortone; Leopoldo Zelante; Massimo Carella; Paola D’Andrea


Book ID
116291513
Publisher
Elsevier Science
Year
2005
Tongue
English
Weight
308 KB
Volume
337
Category
Article
ISSN
0006-291X

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