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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Detaylı Bibliyografya
Asıl Yazarlar: Dutton, Kirsten, Abbas, Leila, Spencer, Joanne, Brannon, Claire, Mowbray, Catriona, Nikaido, Masataka, Kelsh, Robert N., Whitfield, Tanya T.
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: The Company of Biologists Limited 2009
Konular:
Research Article
Online Erişim: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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