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Thyroxine treatments do not correct inner ear defects in tmprss1 mutant mice
Complete deficiency of a member of the type II transmembrane serine protease family, tmprss1 (also known as hepsin), is associated with severe to profound hearing loss in mice and a gross enlargement of the tectorial membrane in the cochlea. Levels of thyroxine in these mice have been shown to be si...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2950264/ https://ncbi.nlm.nih.gov/pubmed/20683358 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/WNR.0b013e32833dbd2d |
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