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A deafness mechanism of digenic Cx26 (GJB2) and Cx30 (GJB6) mutations: Reduction of endocochlear potential by impairment of heterogeneous gap junctional function in the cochlear lateral wall

Digenic Connexin26 (Cx26, GJB2) and Cx30 (GJB6) heterozygous mutations are the second most frequent cause of recessive deafness in humans. However, the underlying deafness mechanism remains unclear. In this study, we created different double Cx26 and Cx30 heterozygous (Cx26(+/−)/Cx30(+/−)) mouse mod...

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Detalhes bibliográficos
Publicado no:Neurobiol Dis
Main Authors: Mei, Ling, Chen, Jin, Zong, Liang, Zhu, Yan, Liang, Chun, Jones, Raleigh O., Zhao, Hong-Bo
Formato: Artigo
Idioma:Inglês
Publicado em: 2017
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5675824/
https://ncbi.nlm.nih.gov/pubmed/28823936
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.nbd.2017.08.002
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