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Peer Review reports

From: Screening of the SLC17A8 gene as a causative factor for autosomal dominant non-syndromic hearing loss in Koreans

Original Submission
26 Aug 2015 Submitted Original manuscript
5 Sep 2015 Author responded Author comments - Nari Ryu
Resubmission - Version 2
5 Sep 2015 Submitted Manuscript version 2
23 Nov 2015 Reviewed Reviewer Report - Karen Pawlowski
24 Nov 2015 Reviewed Reviewer Report - Jung-Bum Shin
29 Nov 2015 Reviewed Reviewer Report - Tahir Atik
21 Dec 2015 Author responded Author comments - Nari Ryu
Resubmission - Version 3
21 Dec 2015 Submitted Manuscript version 3
Publishing
8 Jan 2016 Editorially accepted
22 Jan 2016 Article published 10.1186/s12881-016-0269-3

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