A novel pathogenic variant in OSBPL2 linked to hereditary late-onset deafness in a Mongolian family

Authors

Ningjin Wu, Inner Mongolia University
Husile Husile, Inner Mongolia University
Liqing Yang, Inner Mongolia University
Yaning Cao, Inner Mongolia University
Xing Li, Inner Mongolia University
Wenyan Huo, Inner Mongolia University
Haihua Bai, Inner Mongolia University
Yangjian Liu, Washington University School of Medicine in St. Louis
Qizhu Wu, Inner Mongolia University

Journal

BMC Medical Genetics

Publication Date

3-20-2019

Volume

20

Issue

1

First Page

43

Document Type

Open Access Publication

DOI

10.1186/s12881-019-0781-3

Rights and Permissions

Wu N, Husile H, Yang L, Cao Y, Li X, Huo W, Bai H, Liu Y, Wu Q. A novel pathogenic variant in OSBPL2 linked to hereditary late-onset deafness in a Mongolian family. BMC Med Genet. 2019 Mar 20;20(1):43. doi: 10.1186/s12881-019-0781-3 © The Author(s). 2019 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

Recommended Citation

Wu, Ningjin; Husile, Husile; Yang, Liqing; Cao, Yaning; Li, Xing; Huo, Wenyan; Bai, Haihua; Liu, Yangjian; and Wu, Qizhu, "A novel pathogenic variant in OSBPL2 linked to hereditary late-onset deafness in a Mongolian family." BMC Medical Genetics. 20, 1. 43 (2019).
https://digitalcommons.wustl.edu/open_access_pubs/8161