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A zebrafish model for Waardenburg syndrome type IV reveals diverse roles for Sox10 in the otic vesicle
In humans, mutations in the SOX10 gene are a cause of the auditory-pigmentary disorder Waardenburg syndrome type IV (WS4) and related variants. SOX10 encodes an Sry-related HMG box protein essential for the development of the neural crest; deafness in WS4 and other Waardenburg syndromes is usually a...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
The Company of Biologists Limited
2009
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2615172/ https://ncbi.nlm.nih.gov/pubmed/19132125 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1242/dmm.001164 |
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