Author:
Santarelli Rosamaria,Cama Elona,Scimemi Pietro,Dal Monte Erica,Genovese Elisabetta,Arslan Edoardo
Publisher
Springer Science and Business Media LLC
Subject
General Medicine,Otorhinolaryngology
Reference21 articles.
1. Bicego M, Beltramello M, Melchionda S, Carella M, Piazza V, Zelante V et al (2006) Pathogenetic role of the deafness-related M34T mutation of Cx26. Hum Mol Genet 15:2569–2587
2. Bonfils P, Piron JP, Uziel A, Pujol R (1988) A correlative study of evoked otoacoustic emission properties and audiometric threshold. Arch Otolaryngol 245:53–56
3. Cheng X, Brashears S, Morlet T, Ng SS, Berlin C, Hood L, Keats B (2005) Connexin 26 variants and auditory neuropathy/dys-synchrony among children in schools for the deaf. Am J Med Genet 9999:1–6
4. Cohen-Salmon M, Ott T, Michel V, Hardelin JP, Perfettini I, Eybalin M, Wu T, Marcus DC, Wangemann P, Willecke K, Petit C (2002) Targeted ablation of connexin 26 in the inner ear epithelial gap junction network causes hearing impairment and cell death. Curr Biol 12:1106–1111
5. Cryns K, Orzan E, Murgia A, Huygen PL et al (2004) A genotype-phenotype correlation for GJB2 (connexin 26) deafness. J Med Genet 41:147–154
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