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Peer Review reports

From: Whole exome sequencing revealed a novel homozygous variant in the DGKE catalytic domain: a case report of familial hemolytic uremic syndrome

Original Submission
10 Oct 2019 Submitted Original manuscript
18 Oct 2019 Author responded Author comments - soraya gholizad
Resubmission - Version 2
18 Oct 2019 Submitted Manuscript version 2
4 Dec 2019 Reviewed Reviewer Report - Frédéric Bilan
18 Dec 2019 Reviewed Reviewer Report - Giovanni Malerba
3 Jan 2020 Author responded Author comments - soraya gholizad
Resubmission - Version 3
3 Jan 2020 Submitted Manuscript version 3
20 Jan 2020 Reviewed Reviewer Report - Frédéric Bilan
4 Feb 2020 Reviewed Reviewer Report - Giovanni Malerba
28 Feb 2020 Author responded Author comments - soraya gholizad
Resubmission - Version 4
28 Feb 2020 Submitted Manuscript version 4
25 May 2020 Reviewed Reviewer Report
8 Jun 2020 Author responded Author comments - soraya gholizad
Resubmission - Version 5
8 Jun 2020 Submitted Manuscript version 5
22 Jun 2020 Reviewed Reviewer Report
9 Jul 2020 Author responded Author comments - soraya gholizad
Resubmission - Version 6
9 Jul 2020 Submitted Manuscript version 6
12 Jul 2020 Author responded Author comments - soraya gholizad
Resubmission - Version 7
12 Jul 2020 Submitted Manuscript version 7
Publishing
28 Jul 2020 Editorially accepted
24 Aug 2020 Article published 10.1186/s12881-020-01097-9

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