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GPRASP2, a novel causative gene mutated in an X-linked recessive syndromic hearing loss

Authors

  1. 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
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Citation

Xing G, Yao J, Liu C, et al
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 
May 26, 2017

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