Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report
Pre-publication versions of this article 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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Open peer review is a system where authors know who the reviewers are, and the reviewers know who the authors are. If the manuscript is accepted, the named reviewer reports are published alongside the article. Pre-publication versions of the article are available by contacting firstname.lastname@example.org.
You can find further information about the peer review system here.