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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. Chen DY, et al. Among authors: yu dh. Genet Med. 2017 May;19(5):553-558. doi: 10.1038/gim.2016.142. Epub 2016 Sep 22. Genet Med. 2017. PMID: 27657680 Free article.
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