A novel mutation of X‐linked recessive deafness gene POU3F4 in a boy with congenital deafness
Abstract Purpose To report an interstitial deletion of Xq21.1 in chromosome X in a boy with congenital deafness. Methods The proband underwent a thorough physical examination and a detailed audiological and temporal bone computed tomography (CT) scan. Cochlear implantation was performed on the proba...
| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wiley
2022-08-01
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| Series: | Laryngoscope Investigative Otolaryngology |
| Subjects: | |
| Online Access: | https://doi.org/10.1002/lio2.850 |