A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family

Authors

Haihua Bai, Inner Mongolia University
Xukui Yang, BGI-Shenzhen
Temuribagen, Inner Mongolia University
Guilan, Inner Mongolia University
Suyalatu, Inner Mongolia University
Narisu Narisu, National Institutes of Health
Huiguang Wu, Inner Mongolia University
Yujie Chen, Inner Mongolia University
Yangjian Liu, Washington University School of Medicine in St. Louis
Qizhu Wu, BGI-Shenzhen

Journal

BMC Medical Genetics

Publication Date

2014

Volume

15

Inclusive Pages

34

Document Type

Open Access Publication

Rights and Permissions

Bai et al. BMC Medical Genetics 2014, 15:34 http://www.biomedcentral.com/1471-2350/15/34

Recommended Citation

Bai, Haihua; Yang, Xukui; Temuribagen; Guilan; Suyalatu; Narisu, Narisu; Wu, Huiguang; Chen, Yujie; Liu, Yangjian; and Wu, Qizhu, "A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family." BMC Medical Genetics. 15, 34. (2014).
https://digitalcommons.wustl.edu/open_access_pubs/2572