Targeted Ablation of Connexin26 in the Inner Ear Epithelial Gap Junction Network Causes Hearing Impairment and Cell Death

Mutations in the gene encoding the gap junction protein connexin26 (Cx26) are responsible for the autosomal recessive isolated deafness, DFNB1, which accounts for half of the cases of prelingual profound hereditary deafness in Caucasian populations [1–5]. To date, in vivo approaches to decipher the...

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Detaylı Bibliyografya
Asıl Yazarlar: Cohen-Salmon, Martine, Ott, Thomas, Michel, Vincent, Hardelin, Jean-Pierre, Perfettini, Isabelle, Eybalin, Michel, Wu, Tao, Marcus, Daniel C., Wangemann, Philine, Willecke, Klaus, Petit, Christine
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 2002
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Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC4030438/
https://ncbi.nlm.nih.gov/pubmed/12121617
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