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Whole-exome sequencing identifies a novel missense variant within LOXHD1 causing rare hearing loss in a Chinese family

Published Online: 2019-02-13

Published Print: 2019-12

Authors

Shen, Na

Wang, Ting

Li, Delei

Liu, Aiguo

Lu, Yanjun http://orcid.org/0000-0002-9518-9584
Funding

Funding for this research was provided by:

National Natural Science Foundation of China (81271072)
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Text and Data Mining valid from 2019-02-13
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Article History

Received: 21 November 2018

Accepted: 22 January 2019

First Online: 13 February 2019

Ethics approval and consent to participate

: This study was approved by the Ethics Committee of Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology. Written informed consent were obtained from all subjects.

: All subjects have given their written informed consents for publication of the medical information.

: The authors declare that they have no competing interests.

: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

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