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GPRASP2, a novel causative gene mutated in an X-linked recessive syndromic hearing loss
- Correspondence to Professor Xin Cao, Department of Biotechnology, School of Basic Medical Science, Nanjing Medical University, 101 Longmian Road, Nanjing 211166, China; caoxin{at}njmu.edu.cn
Citation
GPRASP2, a novel causative gene mutated in an X-linked recessive syndromic hearing loss
Publication history
- Received September 20, 2016
- Revised December 5, 2016
- Accepted December 22, 2016
- First published January 17, 2017.
Online issue publication
December 28, 2018
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Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/