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Aberrant Cx26 hemichannels and keratitis-ichthyosis-deafness syndrome: insights into syndromic hearing loss

Mutation of the GJB2 gene, which encodes the connexin 26 (Cx26) gap junction (GJ) protein, is the most common cause of hereditary, sensorineural hearing loss. Cx26 is not expressed in hair cells, but is widely expressed throughout the non-sensory epithelial cells of the cochlea. Most GJB2 mutations...

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書誌詳細
主要な著者: Sanchez, Helmuth A., Verselis, Vytas K.
フォーマット: Artigo
言語:Inglês
出版事項: Frontiers Media S.A. 2014
主題:
オンライン・アクセス:https://ncbi.nlm.nih.gov/pmc/articles/PMC4209889/
https://ncbi.nlm.nih.gov/pubmed/25386120
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fncel.2014.00354
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