A Novel Nonsense Mutation of POU4F3 Gene Causes Autosomal Dominant Hearing Loss
POU4F3 gene encodes a transcription factor which plays an essential role in the maturation and maintenance of hair cells in cochlea and vestibular system. Several mutations of POU4F3 have been reported to cause autosomal dominant nonsyndromic hearing loss in recent years. In this study, we describe...
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Détails bibliographiques
| Publié dans: | Neural plasticity. - 1998. - 2016(2016) vom: 01., Seite 1512831
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| Auteur principal: |
Zhang, Chi
(Auteur) |
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| Autres auteurs: |
Wang, Mingming,
Xiao, Yun,
Zhang, Fengguo,
Zhou, Yicui,
Li, Jianfeng,
Zheng, Qingyin,
Bai, Xiaohui,
Wang, Haibo |
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| Format: | Article en ligne
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| Langue: | English |
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| Publié: |
2016
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| Accès à la collection: | Neural plasticity
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| Sujets: | Journal Article
Codon, Nonsense
Homeodomain Proteins
POU4F3 protein, human
Transcription Factor Brn-3C |
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