Abnormal mRNA Splicing but Normal Auditory Brainstem Response (ABR) in Mice with the Prestin (SLC26A5) IVS2-2A>G mutation

Prestin is critical to OHC somatic motility and hearing sensitivity in mammals. Several mutations of the human SLC26A5 gene have been associated with deafness. However, whether the IVS2-2A>G mutation in the human SLC26A5 gene causes deafness remains controversial. In this study, we created a mous...

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Detalhes bibliográficos
Publicado no:Mutat Res
Main Authors: Zhang, Jian, Liu, Ziyi, Chang, Aoshuang, Fang, Jie, Men, Yuqin, Tian, Yong, Ouyang, Xiaomei, Yan, Denise, Zhang, Aizhen, Sun, Xiaoyang, Tang, Jie, Liu, Xuezhong, Zuo, Jian, Gao, Jiangang
Formato: Artigo
Idioma:Inglês
Publicado em: 2016
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Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5345126/
https://ncbi.nlm.nih.gov/pubmed/27232762
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.mrfmmm.2016.05.004
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