Peer Review reports
From: CUBN gene mutations may cause focal segmental glomerulosclerosis (FSGS) in children
| Original Submission | ||
|---|---|---|
| 27 Jul 2021 | Submitted | Original manuscript |
| 23 Sep 2021 | Reviewed | Reviewer Report |
| 1 Oct 2021 | Reviewed | Reviewer Report |
| 28 Oct 2021 | Author responded | Author comments - Jianhua Zhou |
| Resubmission - Version 2 | ||
| 28 Oct 2021 | Submitted | Manuscript version 2 |
| 3 Nov 2021 | Author responded | Author comments - Jianhua Zhou |
| Resubmission - Version 3 | ||
| 3 Nov 2021 | Submitted | Manuscript version 3 |
| 9 Nov 2021 | Author responded | Author comments - Jianhua Zhou |
| Resubmission - Version 4 | ||
| 9 Nov 2021 | Submitted | Manuscript version 4 |
| 17 Nov 2021 | Reviewed | Reviewer Report |
| 22 Nov 2021 | Reviewed | Reviewer Report |
| 6 Dec 2021 | Author responded | Author comments - Jianhua Zhou |
| Resubmission - Version 5 | ||
| 6 Dec 2021 | Submitted | Manuscript version 5 |
| 17 Dec 2021 | Reviewed | Reviewer Report |
| Resubmission - Version 6 | ||
| Submitted | Manuscript version 6 | |
| Publishing | ||
| 20 Dec 2021 | Editorially accepted | |
| 3 Jan 2022 | Article published | 10.1186/s12882-021-02654-x |
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