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Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family 期刊论文
Journal of Human Genetics, 2015, 卷号: 60, 期号: 3, 页码: 119-126
作者:  Wang, Honghan;  Wang, Xinwei;  He, Chufeng;  Li, Haibo;  Qing, Jie
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