Mutation in the Hair Cell Specific Gene POU4F3 Is a Common Cause for Autosomal Dominant Nonsyndromic Hearing Loss in Chinese Hans
Autosomal dominant nonsyndromic hearing loss (ADNSHL) is extremely heterogeneous. So far the genetic etiological contribution of the gene POU4F3 associated with ADNSHL has been rarely reported. In our previous study, a c.603_604delGG mutation in the hair cell specific gene POU4F3 has been identified...
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Bibliographische Detailangaben
| Veröffentlicht in: | Neural plasticity. - 1998. - 2016(2016) vom: 02., Seite 9890827
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| 1. Verfasser: |
He, Longxia
(VerfasserIn) |
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| Weitere Verfasser: |
Pang, Xiuhong,
Chen, Penghui,
Wu, Hao,
Yang, Tao |
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| Format: | Online-Aufsatz
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| Sprache: | English |
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| Veröffentlicht: |
2016
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| Zugriff auf das übergeordnete Werk: | Neural plasticity
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| Schlagworte: | Journal Article
Homeodomain Proteins
POU4F3 protein, human
Transcription Factor Brn-3C |
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