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Peer Review reports

From: A KRT6A mutation p.Ile462Asn in a Chinese family with pachyonychia congenita, and identification of maternal mosaicism: a case report

Original Submission
17 Jun 2021 Submitted Original manuscript
1 Aug 2021 Reviewed Reviewer Report
2 Aug 2021 Reviewed Reviewer Report
11 Aug 2021 Author responded Author comments - Ming Li
Resubmission - Version 2
11 Aug 2021 Submitted Manuscript version 2
18 Aug 2021 Author responded Author comments - Ming Li
Resubmission - Version 3
18 Aug 2021 Submitted Manuscript version 3
27 Aug 2021 Reviewed Reviewer Report
28 Sep 2021 Author responded Author comments - Ming Li
Resubmission - Version 4
28 Sep 2021 Submitted Manuscript version 4
Resubmission - Version 5
Submitted Manuscript version 5
25 Oct 2021 Reviewed Reviewer Report
Resubmission - Version 6
Submitted Manuscript version 6
Publishing
26 Oct 2021 Editorially accepted
1 Nov 2021 Article published 10.1186/s12920-021-01109-4

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