Works matching AU Wang, Xingwei


Results: 199
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    Exome sequencing identifies a novel CEACAM16 mutation associated with autosomal dominant nonsyndromic hearing loss DFNA4B in a Chinese family.

    Published in:
    Journal of Human Genetics, 2015, v. 60, n. 3, p. 119, doi. 10.1038/jhg.2014.114
    By:
    • Wang, Honghan;
    • Wang, Xinwei;
    • He, Chufeng;
    • Li, Haibo;
    • Qing, Jie;
    • Grati, M'hamed;
    • Hu, Zhengmao;
    • Li, Jiada;
    • Hu, Yiqiao;
    • Xia, Kun;
    • Mei, Lingyun;
    • Wang, Xingwei;
    • Yu, Jianjun;
    • Chen, Hongsheng;
    • Jiang, Lu;
    • Liu, Yalan;
    • Men, Meichao;
    • Zhang, Hailin;
    • Guan, Liping;
    • Xiao, Jingjing
    Publication type:
    Article
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