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Original article
Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss

Authors

  1. Correspondence to Dr Pu Dai, Department of Otolaryngology, Head and Neck Surgery, PLA General Hospital, Beijing, 100853, China; daipu301{at}vip.sina.com
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Citation

Gao X, Yuan Y, Lin Q, et al
Mutation of IFNLR1, an interferon lambda receptor 1, is associated with autosomal-dominant non-syndromic hearing loss

Publication history

  • Received July 28, 2017
  • Revised November 28, 2017
  • Accepted December 11, 2017
  • First published February 16, 2018.

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