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Peer Review reports

From: A rare novel mutation in TECTA causes autosomal dominant nonsyndromic hearing loss in a Mongolian family

Original Submission
10 Nov 2013 Submitted Original manuscript
14 Nov 2013 Author responded Author comments - haihua bai
Resubmission - Version 2
14 Nov 2013 Submitted Manuscript version 2
10 Dec 2013 Reviewed Reviewer Report - Oscar DIAZ HORTA
26 Dec 2013 Reviewed Reviewer Report - Miguel Moreno-Pelayo
2 Mar 2014 Author responded Author comments - haihua bai
Resubmission - Version 3
2 Mar 2014 Submitted Manuscript version 3
Publishing
12 Mar 2014 Editorially accepted
19 Mar 2014 Article published 10.1186/1471-2350-15-34

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