A dominant variant in DMXL2 is linked to nonsyndromic hearing loss.

Dong-Ye ChenXing-Feng LiuXiao-Jiang LinDan ZhangYong-Chuan ChaiDe-Hong YuChang-Ling SunXue-Ling WangWei-Dong ZhuYing ChenLian-Hua SunXiao-Wen WangFu-Xin ShiZhi-Wu HuangTao YangHao Wu

Published in: Genetics in medicine : official journal of the American College of Medical Genetics (2016)

Our data indicated that the p.Arg2417His variant in DMXL2 is associated with dominant, nonsyndromic hearing loss and suggested an important role of DMXL2 in inner ear function.Genet Med advance online publication 22 September 2016.

Keyphrases

hearing loss
electronic health record
social media
health information
deep learning