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Eya1 regulates the growth of otic epithelium and interacts with Pax2 during the development of all sensory areas in the inner ear
Members of the Eyes absent (Eya) gene family are important for auditory system development. While mutations in human EYA4 cause late-onset deafness at the DFNA10 locus, mutations in human EYA1 cause branchio–oto–renal (BOR) syndrome. Inactivation of Eya1 in mice causes an early arrest of the inner e...
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| Asıl Yazarlar: | , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
2006
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3882145/ https://ncbi.nlm.nih.gov/pubmed/16916509 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ydbio.2006.06.049 |
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