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Peer Review reports

From: A de novo SCN8A heterozygous mutation in a child with epileptic encephalopathy: a case report

Original Submission
27 Jan 2018 Submitted Original manuscript
14 Oct 2018 Reviewed Reviewer Report - Wenhao Zhou
21 Nov 2018 Reviewed Reviewer Report - Elena Gardella
27 May 2019 Author responded Author comments - Kao-min Lin
Resubmission - Version 2
27 May 2019 Submitted Manuscript version 2
4 Jun 2019 Reviewed Reviewer Report - Elena Gardella
26 Aug 2019 Reviewed Reviewer Report - Reviewer 2
8 Sep 2019 Author responded Author comments - Kao-min Lin
Resubmission - Version 3
8 Sep 2019 Submitted Manuscript version 3
10 Oct 2019 Author responded Author comments - Kao-min Lin
Resubmission - Version 4
10 Oct 2019 Submitted Manuscript version 4
15 Oct 2019 Author responded Author comments - Kao-min Lin
Resubmission - Version 5
15 Oct 2019 Submitted Manuscript version 5
Publishing
21 Oct 2019 Editorially accepted
1 Nov 2019 Article published 10.1186/s12887-019-1796-9

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