Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8806373 | International Journal of Pediatric Otorhinolaryngology | 2018 | 7 Pages |
Abstract
Our findings strongly suggest that the c.2389Gâ¯>â¯A mutation in WFS1 is associated with all-frequency hearing loss, rather than low- or high-frequency loss. So far, the mutation is only reported in Chinese. Prenatal diagnosis and prenatal counseling is available for these two Chinese families.
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Authors
Hongbo Cheng, Qin Zhang, Wenbin Wang, Qingxia Meng, Fuxin Wang, Minjuan Liu, Jun Mao, Yichao Shi, Wei Wang, Hong Li,