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

Issued Date

2019-09-20

Resource Type

Letter

ISSN

18735533
16738527

DOI

10.1016/j.jgg.2019.09.003

Other identifier(s)

2-s2.0-85075078839

Rights

Mahidol University

Rights Holder(s)

SCOPUS

Bibliographic Citation

Journal of Genetics and Genomics. Vol.46, No.9 (2019), 445-449

Suggested 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. Journal of Genetics and Genomics. Vol.46, No.9 (2019), 445-449. doi:10.1016/j.jgg.2019.09.003 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/50079

Research Projects

Organizational Units

Authors

Journal Issue

Thesis

Title

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

Author(s)

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

Other Contributor(s)

School of Life Sciences Fudan University
 Zhengzhou University
 Brigham and Women's Hospital
 Faculty of Medicine, Ramathibodi Hospital, Mahidol University
 Fudan University
 Harvard Medical School Center for Hereditary Deafness
 Shanghai Institute for Biological Sciences Chinese Academy of Sciences

Keyword(s)

Biochemistry, Genetics and Molecular Biology

Availability

URI

https://repository.li.mahidol.ac.th/handle/20.500.14594/50079

Collections

Scopus 2019