GATA3 controls the specification of prosensory domain and neuronal survival in the mouse cochlea

HDR syndrome (also known as Barakat syndrome) is a developmental disorder characterized by hypoparathyroidism, sensorineural deafness and renal disease. Although genetic mapping and subsequent functional studies indicate that GATA3 haplo-insufficiency causes human HDR syndrome, the role of Gata3 in...

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Main Authors: Luo, Xiong-jian, Deng, Min, Xie, Xiaoling, Huang, Liang, Wang, Hui, Jiang, Lichun, Liang, Guoqing, Hu, Fang, Tieu, Roger, Chen, Rui, Gan, Lin
Formato: Artigo
Idioma:Inglês
Publicado em: Oxford University Press 2013
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Articles
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3749857/
https://ncbi.nlm.nih.gov/pubmed/23666531
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddt212
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