Functional Correlation of Two Novel Nonsense POU4F3 Mutations Causing Late‐Onset Progressive Nonsyndromic Hearing Loss in DFNA15 Families
ABSTRACT Background POU4F3 mutations cause DFNA15, an autosomal dominant nonsyndromic hearing loss. POU4F3 encodes a transcription factor crucial for inner ear hair cell development and maintenance. Objective To identify and functionally characterize novel POU4F3 mutations in two Chinese families wi...
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| Main Authors: | , , , |
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| Format: | Article |
| Language: | English |
| Published: |
Wiley
2025-05-01
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| Series: | Molecular Genetics & Genomic Medicine |
| Subjects: | |
| Online Access: | https://doi.org/10.1002/mgg3.70100 |
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