A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family (Q35204053)
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| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family |
scientific article |
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A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family (English)
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Haihua Bai
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Xukui Yang
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Temuribagen
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Guilan
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Suyalatu
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Narisu
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Huiguang Wu
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Yujie Chen
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Yangjian Liu
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Qizhu Wu
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19 March 2014
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34
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