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Peer Review reports

From: Paroxysmal extreme pain disorder in family with c.3892G > T (p.Val1298Phe) in the SCN9A gene mutation – case report

Original Submission
29 Aug 2019 Submitted Original manuscript
10 Oct 2019 Author responded Author comments - Adam Stępień
1 Dec 2019 Reviewed Reviewer Report
21 Jan 2020 Reviewed Reviewer Report
24 Feb 2020 Author responded Author comments - Adam Stępień
Resubmission - Version 2
10 Oct 2019 Submitted Manuscript version 2
20 Mar 2020 Reviewed Reviewer Report
29 Mar 2020 Reviewed Reviewer Report
27 Apr 2020 Author responded Author comments - Adam Stępień
Resubmission - Version 3
27 Apr 2020 Submitted Manuscript version 3
4 May 2020 Author responded Author comments - Adam Stępień
Resubmission - Version 4
4 May 2020 Submitted Manuscript version 4
Publishing
7 May 2020 Editorially accepted
13 May 2020 Article published 10.1186/s12883-020-01770-9

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