Peer Review reports
From: Distinct clinical phenotypes in a family with a novel truncating MEN1 frameshift mutation
| Original Submission | ||
|---|---|---|
| 7 Sep 2021 | Submitted | Original manuscript |
| 11 Nov 2021 | Reviewed | Reviewer Report |
| 30 Nov 2021 | Reviewed | Reviewer Report |
| 21 Jan 2022 | Author responded | Author comments - Christoph Welsch |
| Resubmission - Version 2 | ||
| 21 Jan 2022 | Submitted | Manuscript version 2 |
| 28 Jan 2022 | Reviewed | Reviewer Report |
| 18 Feb 2022 | Author responded | Author comments - Christoph Welsch |
| Resubmission - Version 3 | ||
| 18 Feb 2022 | Submitted | Manuscript version 3 |
| Publishing | ||
| 2 Mar 2022 | Editorially accepted | |
| 14 Mar 2022 | Article published | 10.1186/s12902-022-00978-9 |
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