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Peer Review reports

From: Novel ECHS1 mutations in Leigh syndrome identified by whole-exome sequencing in five Chinese families: case report

Original Submission
11 Oct 2019 Submitted Original manuscript
21 Oct 2019 Author responded Author comments - Dan Sun
Resubmission - Version 2
21 Oct 2019 Submitted Manuscript version 2
15 Nov 2019 Author responded Author comments - Dan Sun
Resubmission - Version 3
15 Nov 2019 Submitted Manuscript version 3
2 Feb 2020 Reviewed Reviewer Report
11 Mar 2020 Reviewed Reviewer Report
29 Apr 2020 Author responded Author comments - Dan Sun
Resubmission - Version 4
29 Apr 2020 Submitted Manuscript version 4
4 May 2020 Reviewed Reviewer Report
26 May 2020 Reviewed Reviewer Report
9 Jun 2020 Author responded Author comments - Dan Sun
Resubmission - Version 5
9 Jun 2020 Submitted Manuscript version 5
19 Jun 2020 Author responded Author comments - Dan Sun
Resubmission - Version 6
19 Jun 2020 Submitted Manuscript version 6
27 Jun 2020 Author responded Author comments - Dan Sun
Resubmission - Version 7
27 Jun 2020 Submitted Manuscript version 7
Publishing
1 Jul 2020 Editorially accepted
16 Jul 2020 Article published 10.1186/s12881-020-01083-1

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