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Dominant connexin26 mutants associated with human hearing loss have trans-dominant effects on connexin30
Dominant mutations in GJB2, the gene encoding the human gap junction protein connexin26 (Cx26), cause hearing loss. We investigated whether dominant Cx26 mutants interact directly with Cx30. HeLa cells stably expressing nine dominant Cx26 mutants, six associated with non-syndromic hearing loss (W44C...
Tallennettuna:
| Päätekijät: | , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2010
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| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2868926/ https://ncbi.nlm.nih.gov/pubmed/20096356 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2010.01.010 |
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