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Four Novel Variants in POU4F3 Cause Autosomal Dominant Nonsyndromic Hearing Loss
Hereditary hearing loss is one of the most common sensory disabilities worldwide. Mutation of POU domain class 4 transcription factor 3 (POU4F3) is considered the pathogenic cause of autosomal dominant nonsyndromic hearing loss (ADNSHL), designated as autosomal dominant nonsyndromic deafness 15. In...
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| Yayımlandı: | Neural Plast |
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| Asıl Yazarlar: | , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Hindawi
2020
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7349627/ https://ncbi.nlm.nih.gov/pubmed/32684921 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1155/2020/6137083 |
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