This article has Open Peer Review reports available.
Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report
- Hye Ji Choi†1,
- Joon Suk Lee†2,
- Seyoung Yu2,
- Do Hyeon Cha2,
- Heon Yung Gee2,
- Jae Young Choi1,
- Jong Dae Lee3Email author and
- Jinsei Jung1, 4Email authorView ORCID ID profile
© The Author(s). 2017
Received: 3 July 2017
Accepted: 8 December 2017
Published: 19 December 2017
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting email@example.com.
|3 Jul 2017||Submitted||Original manuscript|
|8 Aug 2017||Reviewed||Reviewer Report - Karen Friderici|
|3 Oct 2017||Reviewed||Reviewer Report - Trevor Lucas|
|12 Nov 2017||Author responded||Author comments - Hye Ji Choi|
|Resubmission - Version 2|
|12 Nov 2017||Submitted||Manuscript version 2|
|28 Nov 2017||Reviewed||Reviewer Report - Trevor Lucas|
|5 Dec 2017||Reviewed||Reviewer Report - Karen Friderici|
|8 Dec 2017||Author responded||Author comments - Hye Ji Choi|
|Resubmission - Version 3|
|8 Dec 2017||Submitted||Manuscript version 3|
|8 Dec 2017||Editorially accepted|
|19 Dec 2017||Article published||10.1186/s12881-017-0511-7|
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