Exome sequencing identifies a novel missense mutation of...

International Journal of Pediatric Otorhinolaryngology 2017 / 09 Vol. 100

Exome sequencing identifies a novel missense mutation of WFS1 as the cause of non-syndromic low-frequency hearing loss in a Chinese family

Niu, Zhijie, Feng, Yong, Hu, Zhengmao, Li, Jiada, Sun, Jie, Chen, Hongsheng, He, Chufeng, Wang, Xueping, Jiang, Lu, Liu, Yalan, Cai, Xinzhang, Wang, Lili, Cai, Yuxiang, Liu, Xuezhong, Mei, Lingyun
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Volume:
100
Language:
english
Journal:
International Journal of Pediatric Otorhinolaryngology
DOI:
10.1016/j.ijporl.2017.06.008
Date:
September, 2017
File:
PDF, 1.27 MB
english, 2017
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