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Peer Review reports

From: A novel pore-region mutation, c.887G > A (p.G296D) in KCNQ4, causing hearing loss in a Chinese family with autosomal dominant non-syndromic deafness 2

Original Submission
16 Aug 2016 Submitted Original manuscript
16 Nov 2016 Reviewed Reviewer Report - Jeffrey Holt
18 Nov 2016 Reviewed Reviewer Report - Regina Celia Mingroni Netto
19 Dec 2016 Author responded Author comments - Bangqing Huang
Resubmission - Version 2
19 Dec 2016 Submitted Manuscript version 2
16 Jan 2017 Reviewed Reviewer Report - Jeffrey Holt
25 Jan 2017 Reviewed Reviewer Report - Regina Celia Mingroni Netto
3 Feb 2017 Author responded Author comments - Bangqing Huang
Resubmission - Version 3
3 Feb 2017 Submitted Manuscript version 3
7 Mar 2017 Author responded Author comments - Bangqing Huang
Resubmission - Version 4
7 Mar 2017 Submitted Manuscript version 4
Publishing
8 Mar 2017 Editorially accepted
24 Mar 2017 Article published 10.1186/s12881-017-0396-5

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