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Peer Review reports

From: A novel splice site variant c.1183 + 1 G > C in DFNA5 causing autosomal dominant nonsyndromic hearing loss in a Chinese family

Original Submission
17 Mar 2022 Submitted Original manuscript
18 Apr 2022 Reviewed Reviewer Report
19 Apr 2022 Reviewed Reviewer Report
6 May 2022 Author responded Author comments - Dingjun Zha
Resubmission - Version 2
6 May 2022 Submitted Manuscript version 2
9 May 2022 Author responded Author comments - Dingjun Zha
Resubmission - Version 3
9 May 2022 Submitted Manuscript version 3
10 May 2022 Author responded Author comments - Dingjun Zha
Resubmission - Version 4
10 May 2022 Submitted Manuscript version 4
26 May 2022 Reviewed Reviewer Report
10 Jun 2022 Reviewed Reviewer Report
5 Jul 2022 Author responded Author comments - Dingjun Zha
Resubmission - Version 5
5 Jul 2022 Submitted Manuscript version 5
Publishing
11 Jul 2022 Editorially accepted
21 Jul 2022 Article published 10.1186/s12920-022-01315-8

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