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Clinical and Molecular Aspects Associated with Defects in the Transcription Factor POU3F4: A Review
X-linked deafness (DFNX) is estimated to account for up to 2% of cases of hereditary hearing loss and occurs in both syndromic and non-syndromic forms. POU3F4 is the gene most commonly associated with X-linked deafness (DFNX2, DFN3) and accounts for about 50% of the cases of X-linked non-syndromic h...
| Autores principales: | , , , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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MDPI
2023
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10296620/ https://www.ncbi.nlm.nih.gov/pubmed/37371790 http://dx.doi.org/10.3390/biomedicines11061695 |