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

标题
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
作者
关键词
Gap junction, Connexin, Cx26, Cx30, Endocochlear potential, Deafness, Cochlea
出版物
NEUROBIOLOGY OF DISEASE
Volume 108, Issue -, Pages 195-203
出版商
Elsevier BV
发表日期
2017-08-17
DOI
10.1016/j.nbd.2017.08.002

向作者/读者发起求助以获取更多资源

Reprint

联系作者

Find Funding. Review Successful Grants.

Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.

Explore

Find the ideal target journal for your manuscript

Explore over 38,000 international journals covering a vast array of academic fields.

Search