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

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Bibliographic Details
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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