Peer Review reports
From: Novel SETBP1 mutation in a chinese family with intellectual disability
| Original Submission | ||
|---|---|---|
| 1 Mar 2023 | Submitted | Original manuscript |
| Resubmission - Version 2 | ||
| Submitted | Manuscript version 2 | |
| Resubmission - Version 3 | ||
| Submitted | Manuscript version 3 | |
| Resubmission - Version 4 | ||
| Submitted | Manuscript version 4 | |
| 5 Jun 2023 | Reviewed | Reviewer Report |
| 28 Jun 2023 | Reviewed | Reviewer Report |
| 4 Jul 2023 | Author responded | Author comments - Hong‐Mei Xiao |
| Resubmission - Version 5 | ||
| 4 Jul 2023 | Submitted | Manuscript version 5 |
| 8 Jul 2023 | Author responded | Author comments - Hong‐Mei Xiao |
| Resubmission - Version 6 | ||
| 8 Jul 2023 | Submitted | Manuscript version 6 |
| 14 Jul 2023 | Author responded | Author comments - Hong‐Mei Xiao |
| Resubmission - Version 7 | ||
| 14 Jul 2023 | Submitted | Manuscript version 7 |
| 10 Aug 2023 | Reviewed | Reviewer Report |
| 26 Aug 2023 | Author responded | Author comments - Hong‐Mei Xiao |
| Resubmission - Version 8 | ||
| 26 Aug 2023 | Submitted | Manuscript version 8 |
| Publishing | ||
| 28 Aug 2023 | Editorially accepted | |
| 5 Oct 2023 | Article published | 10.1186/s12920-023-01649-x |
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