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Peer Review reports

From: Exome sequencing contributes to identify comorbidities in a rare case of infant ARDS induced by the CD40LG mutation

Original Submission
23 Aug 2021 Submitted Original manuscript
29 Aug 2021 Author responded Author comments - Xue Gong
Resubmission - Version 2
29 Aug 2021 Submitted Manuscript version 2
26 Feb 2022 Reviewed Reviewer Report
7 Mar 2022 Reviewed Reviewer Report
30 Mar 2022 Author responded Author comments - Xue Gong
Resubmission - Version 3
30 Mar 2022 Submitted Manuscript version 3
8 Apr 2022 Reviewed Reviewer Report
21 Apr 2022 Reviewed Reviewer Report
5 May 2022 Author responded Author comments - Xue Gong
Resubmission - Version 4
5 May 2022 Submitted Manuscript version 4
11 May 2022 Author responded Author comments - Xue Gong
Resubmission - Version 5
11 May 2022 Submitted Manuscript version 5
17 May 2022 Author responded Author comments - Xue Gong
Resubmission - Version 6
17 May 2022 Submitted Manuscript version 6
15 Jun 2022 Author responded Author comments - Xue Gong
Resubmission - Version 7
15 Jun 2022 Submitted Manuscript version 7
17 Jun 2022 Author responded Author comments - Xue Gong
Resubmission - Version 8
17 Jun 2022 Submitted Manuscript version 8
26 Jun 2022 Author responded Author comments - Xue Gong
Resubmission - Version 9
26 Jun 2022 Submitted Manuscript version 9
Publishing
1 Jul 2022 Editorially accepted
8 Jul 2022 Article published 10.1186/s12920-022-01303-y

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