This gene encodes a member of the gap junction protein family. The gap junctions were first characterized by electron microscopy as regionally specialized structures on plasma membranes of contacting
We report application of RNA-seq for transcriptomic analyses of cochlear tissues from wildtype and DFNA15 deafness mouse model Pou4f3(Δ/+) to reveal gene expressions altered by Pou4f3 mutation Overall
A Chinese family from Hainan Province experienced non-syndromic hearing loss (NSHL). Peripheral venous blood samples were collected from 18 members of this family, and DNA was extracted for whole-exom
