Peer Review reports
From: The first case of intellectual disability caused by novel compound heterozygosity for NUDT2 variants
| Original Submission | ||
|---|---|---|
| 16 Jul 2023 | Submitted | Original manuscript |
| Resubmission - Version 2 | ||
| Submitted | Manuscript version 2 | |
| Resubmission - Version 3 | ||
| Submitted | Manuscript version 3 | |
| 26 Nov 2023 | Reviewed | Reviewer Report |
| 12 Dec 2023 | Reviewed | Reviewer Report |
| 19 Dec 2023 | Author responded | Author comments - Hongmin Zhu |
| Resubmission - Version 4 | ||
| 19 Dec 2023 | Submitted | Manuscript version 4 |
| 21 Dec 2023 | Author responded | Author comments - Hongmin Zhu |
| Resubmission - Version 5 | ||
| 21 Dec 2023 | Submitted | Manuscript version 5 |
| 5 Jan 2024 | Reviewed | Reviewer Report |
| Resubmission - Version 6 | ||
| Submitted | Manuscript version 6 | |
| Publishing | ||
| 8 Jan 2024 | Editorially accepted | |
| 19 Jan 2024 | Article published | 10.1186/s12887-024-04542-3 |
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