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Peer Review reports

From: A novel MYH14 mutation in a Chinese family with autosomal dominant nonsyndromic hearing loss

Original Submission
18 Dec 2019 Submitted Original manuscript
6 Jan 2020 Author responded Author comments - Mingming Wang
Resubmission - Version 2
6 Jan 2020 Submitted Manuscript version 2
14 Mar 2020 Reviewed Reviewer Report - Barbara Vona
16 Mar 2020 Reviewed Reviewer Report - Khurram Liaqat
14 Apr 2020 Author responded Author comments - Mingming Wang
Resubmission - Version 3
14 Apr 2020 Submitted Manuscript version 3
19 Apr 2020 Reviewed Reviewer Report - Barbara Vona
13 May 2020 Author responded Author comments - Mingming Wang
Resubmission - Version 4
13 May 2020 Submitted Manuscript version 4
21 May 2020 Reviewed Reviewer Report - Barbara Vona
27 May 2020 Author responded Author comments - Mingming Wang
Resubmission - Version 5
27 May 2020 Submitted Manuscript version 5
13 Jun 2020 Author responded Author comments - Mingming Wang
Resubmission - Version 6
13 Jun 2020 Submitted Manuscript version 6
19 Jun 2020 Author responded Author comments - Mingming Wang
Resubmission - Version 7
19 Jun 2020 Submitted Manuscript version 7
24 Jun 2020 Author responded Author comments - Mingming Wang
Resubmission - Version 8
24 Jun 2020 Submitted Manuscript version 8
29 Jun 2020 Author responded Author comments - Mingming Wang
Resubmission - Version 9
29 Jun 2020 Submitted Manuscript version 9
1 Jul 2020 Author responded Author comments - Mingming Wang
Resubmission - Version 10
1 Jul 2020 Submitted Manuscript version 10
Publishing
2 Jul 2020 Editorially accepted
25 Jul 2020 Article published 10.1186/s12881-020-01086-y

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