Skip to main content

Peer Review reports

From: Whole-exome sequencing identified a missense mutation in WFS1 causing low-frequency hearing loss: a case report

Original Submission
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
Publishing
8 Dec 2017 Editorially accepted
19 Dec 2017 Article published 10.1186/s12881-017-0511-7

You can find further information about peer review here.

Back to article page