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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 |
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Title: |
The p.(Pro170Leu) variant in NOG impairs noggin secretion and causes autosomal dominant congenital conductive hearing loss due to stapes ankylosis |
Author: |
Shu, Yilai Wang, Lijun Cheng, Xiaoting Tangshewinsirikul, Chayada Shi, Weili Yuan, Yasheng Yan, Zhiqiang Li, Huawei Shen, Jun Chen, Bing Zou, Weiguo |
Appeared in: |
Journal of genetics and genomics |
Paging: |
Volume 46 () nr. 9 pages 445-449 |
Year: |
2019 |
Contents: |
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Publisher: |
Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, and Genetics Society of China |
Source file: |
Elektronische Wetenschappelijke Tijdschriften |
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