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A novel compound heterozygous mutation in the GJB2 gene is associated with non-syndromic hearing loss in a Chinese family.

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Title: A novel compound heterozygous mutation in the GJB2 gene is associated with non-syndromic hearing loss in a Chinese family.
Authors: Haiou Jiang1 hhjiangh@126.com, Youya Niu1, Lingfeng Qu1, Xueshuang Huang1, Xinlong Zhu1, Genyun Tang1
Source: BioScience Trends. Oct2018, Vol. 12 Issue 5, p470-475. 6p.
Database: Academic Search Ultimate
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  Data: A novel compound heterozygous mutation in the GJB2 gene is associated with non-syndromic hearing loss in a Chinese family.
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  Data: <searchLink fieldCode="AR" term="%22Haiou+Jiang%22">Haiou Jiang</searchLink><relatesTo>1</relatesTo><i> hhjiangh@126.com</i><br /><searchLink fieldCode="AR" term="%22Youya+Niu%22">Youya Niu</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Lingfeng+Qu%22">Lingfeng Qu</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Xueshuang+Huang%22">Xueshuang Huang</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Xinlong+Zhu%22">Xinlong Zhu</searchLink><relatesTo>1</relatesTo><br /><searchLink fieldCode="AR" term="%22Genyun+Tang%22">Genyun Tang</searchLink><relatesTo>1</relatesTo>
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  Data: <searchLink fieldCode="JN" term="%22BioScience+Trends%22">BioScience Trends</searchLink>. Oct2018, Vol. 12 Issue 5, p470-475. 6p.
PLink https://search.ebscohost.com/login.aspx?direct=true&site=eds-live&db=asn&AN=133202262
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        Value: 10.5582/bst.2018.01156
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        Text: English
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              Text: Oct2018
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