A novel pathogenic variant in OSBPL2 linked to hereditary late-onset deafness in a Mongolian family
BMC Medical Genetics
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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.
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).