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Peer Review reports

From: Severe phenotypes of B3GAT3-related disorder caused by two heterozygous variants: a case report and literature review

Original Submission
14 Nov 2020 Submitted Original manuscript
22 Feb 2021 Reviewed Reviewer Report
16 Mar 2021 Reviewed Reviewer Report
14 Apr 2021 Author responded Author comments - Ying Li
Resubmission - Version 2
14 Apr 2021 Submitted Manuscript version 2
26 May 2021 Reviewed Reviewer Report
17 Jun 2021 Author responded Author comments - Ying Li
Resubmission - Version 3
17 Jun 2021 Submitted Manuscript version 3
14 Jul 2021 Author responded Author comments - Ying Li
Resubmission - Version 4
14 Jul 2021 Submitted Manuscript version 4
16 Jul 2021 Author responded Author comments - Ying Li
Resubmission - Version 5
16 Jul 2021 Submitted Manuscript version 5
26 Sep 2021 Author responded Author comments - Ying Li
Resubmission - Version 6
26 Sep 2021 Submitted Manuscript version 6
4 Oct 2021 Author responded Author comments - Ying Li
Resubmission - Version 7
4 Oct 2021 Submitted Manuscript version 7
11 Oct 2021 Author responded Author comments - Ying Li
Resubmission - Version 8
11 Oct 2021 Submitted Manuscript version 8
4 Jan 2022 Author responded Author comments - Ying Li
Resubmission - Version 9
4 Jan 2022 Submitted Manuscript version 9
Publishing
10 Jan 2022 Editorially accepted
12 Feb 2022 Article published 10.1186/s12920-022-01160-9

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