Connexin30-Deficiency Causes Mild Hearing Loss With the Reduction of Endocochlear Potential and ATP Release

GJB2 and GJB6 are adjacent genes encoding connexin 26 (Cx26) and connexin 30 (Cx30), respectively, with overlapping expressions in the inner ear. Both genes are associated with the commonest monogenic hearing disorder, recessive isolated deafness DFNB1. Cx26 plays an important role in auditory devel...

Deskribapen osoa

Xehetasun bibliografikoak

Egile Nagusiak:	Junmin Chen, Penghui Chen, Baihui He, Tianyu Gong, Yue Li, Jifang Zhang, Jingrong Lv, Fabio Mammano, Shule Hou, Jun Yang
Formatua:	Artigo
Hizkuntza:	Inglês
Argitaratua:	Frontiers Media S.A. 2022-01-01
Saila:	Frontiers in Cellular Neuroscience
Gaiak:	connexin30 hearing loss connexin26 stria vascularis endocochlear potential
Sarrera elektronikoa:	https://www.frontiersin.org/articles/10.3389/fncel.2021.819194/full
Etiketak:	Etiketa erantsi Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!