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Eya1 gene dosage critically affects the development of sensory epithelia in the mammalian inner ear
Haploinsufficiency of the transcription co-activator EYA1 causes branchio–oto–renal syndrome, congenital birth defects that account for as many as 2% of profoundly deaf children; however, the underlying cause for its dosage requirement and its specific role in sensory cell development of the inner e...
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| Autori principali: | , , , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Oxford University Press
2008
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2722896/ https://ncbi.nlm.nih.gov/pubmed/18678597 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddn229 |
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