Three MYO15A Mutations Identified in One Chinese Family with Autosomal Recessive Nonsyndromic Hearing Loss
Hearing impairment is one of the most common sensory disease, of which more than 50% is attributed to a genetic etiology. The goal of this research is to explore the genetic cause of a Chinese deafness pedigree who was excluded of GJB2, SLC26A4, or MtDNA12SrRNA variants. Three variants, c.3971C>A...
Ausführliche Beschreibung
Bibliographische Detailangaben
| Veröffentlicht in: | Neural plasticity. - 1998. - 2018(2018) vom: 30., Seite 5898025
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| 1. Verfasser: |
Zhang, Fengguo
(VerfasserIn) |
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| Weitere Verfasser: |
Xu, Lei,
Xiao, Yun,
Li, Jianfeng,
Bai, Xiaohui,
Wang, Haibo |
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| Format: | Online-Aufsatz
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| Sprache: | English |
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| Veröffentlicht: |
2018
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| Zugriff auf das übergeordnete Werk: | Neural plasticity
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| Schlagworte: | Journal Article
Research Support, Non-U.S. Gov't
MYO15A protein, human
Mutant Proteins
Myosins
EC 3.6.4.1 |
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