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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(...
| Autores principales: | , , , , , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2006
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1796619/ https://www.ncbi.nlm.nih.gov/pubmed/17187680 http://dx.doi.org/10.1186/1741-7015-4-37 |