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Macrophage invasion contributes to degeneration of stria vascularis in Pendred syndrome mouse model
BACKGROUND: Pendred syndrome, an autosomal-recessive disorder characterized by deafness and goiter, is caused by a mutation of SLC26A4, which codes for the anion exchanger pendrin. We investigated the relationship between pendrin expression and deafness using mice that have (Slc26a4(+/+ )or Slc26a4(...
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| Main Authors: | , , , , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
BioMed Central
2006
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| Fag: | |
| Online adgang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1796619/ https://ncbi.nlm.nih.gov/pubmed/17187680 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1741-7015-4-37 |
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