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A Deafness Associated Mutant Human Connexin 26 Improves The Epithelial Barrier In Vitro
A large proportion of recessive non-syndromic hearing loss is due to mutations in the GJB2 gene encoding connexin 26 (Cx26), a component of a gap junction. Within different ethnic groups there are specific common recessive mutations each with a relatively high carrier frequency suggesting a possibil...
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| 主要な著者: | , , , , , , , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
2007
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2845879/ https://ncbi.nlm.nih.gov/pubmed/17581693 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s00232-007-9025-0 |
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