Citations for
1DFNA71, DMXL2
A dominant variant in DMXL2 is linked to nonsyndromic hearing loss
Chen DY, Liu XF, Lin XJ, Zhang D, Chai YC, Yu DH, Sun CL, Wang XL, Zhu WD, Chen Y, Sun LH, Wang XW, Shi FX, Huang ZW, Yang T, Wu H
Genet Med. May;19(5):553-558. doi: 10.1038/gim.2016.142. Epub 2016 Sep 22 2017