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The p.(Pro170Leu) variant in NOG impairs noggin secretion and causes autosomal dominant congenital conductive hearing loss due to stapes ankylosis

Yilai Shu Lijun Wang Xiaoting Cheng Chayada Tangshewinsirikul Weili Shi Yasheng Yuan Zhiqiang Yan Huawei Li Jun Shen Bing Chen Weiguo Zou

Yilai Shu, Lijun Wang, Xiaoting Cheng, Chayada Tangshewinsirikul, Weili Shi, Yasheng Yuan, Zhiqiang Yan, Huawei Li, Jun Shen, Bing Chen, Weiguo Zou. The p.(Pro170Leu) variant in NOG impairs noggin secretion and causes autosomal dominant congenital conductive hearing loss due to stapes ankylosis[J]. Journal of Genetics and Genomics, 2019, 46(9): 445-449. doi: 10.1016/j.jgg.2019.09.003
Citation: Yilai Shu, Lijun Wang, Xiaoting Cheng, Chayada Tangshewinsirikul, Weili Shi, Yasheng Yuan, Zhiqiang Yan, Huawei Li, Jun Shen, Bing Chen, Weiguo Zou. The p.(Pro170Leu) variant in NOG impairs noggin secretion and causes autosomal dominant congenital conductive hearing loss due to stapes ankylosis[J]. Journal of Genetics and Genomics, 2019, 46(9): 445-449. doi: 10.1016/j.jgg.2019.09.003

doi: 10.1016/j.jgg.2019.09.003

The p.(Pro170Leu) variant in NOG impairs noggin secretion and causes autosomal dominant congenital conductive hearing loss due to stapes ankylosis

More Information
  • These authors contributed equally to this work.
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出版历程
  • 收稿日期:  2019-04-17
  • 录用日期:  2019-09-11
  • 修回日期:  2019-08-17
  • 网络出版日期:  2019-09-27
  • 刊出日期:  2019-09-20

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