Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family.
Niu Z, Feng Y, Hu Z, Li J, Sun J, Chen H, He C, Wang X, Jiang L, Liu Y, Cai X, Wang L, Cai Y, Liu X, Mei L.
Niu Z, et al. Among authors: cai x, cai y.
Int J Pediatr Otorhinolaryngol. 2017 Sep;100:1-7. doi: 10.1016/j.ijporl.2017.06.008. Epub 2017 Jun 15.
Int J Pediatr Otorhinolaryngol. 2017.
PMID: 28802351