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Trafficking abnormality and ER stress underlie functional deficiency of hearing impairmentassociated connexin-31 mutants
Hearing impairment (HI) affects 1/1000 children and over 2% of the aged population. We have previously reported that mutations in the gene encoding gap junction protein connexin-31 (C×31) are associated with HI. The pathological mechanism of the disease mutations remains unknown. Here, we show that...
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| Publicado no: | Protein Cell |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Higher Education Press
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4875122/ https://ncbi.nlm.nih.gov/pubmed/21204020 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s13238-010-0118-7 |
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