| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8806428 | International Journal of Pediatric Otorhinolaryngology | 2018 | 4 Pages |
Abstract
We report the first SMPX (DFNX4) mutation in a North American family. Our findings contribute to the existing genotypic and phenotypic spectrum of SMPX associated hearing loss. Furthermore, our data suggest that exome sequencing is promising in the genetic diagnosis of hearing loss.
Keywords
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Authors
Zhijie Niu, Denise Yan, Sara Bressler, Lingyun Mei, Yong Feng, Xuezhong Liu,