Peer Review reports
From: A novel SLC12A3 homozygous c2039delG mutation in Gitelman syndrome with hypocalcemia
| Original Submission | ||
|---|---|---|
| 10 Mar 2018 | Submitted | Original manuscript |
| 9 Jul 2018 | Reviewed | Reviewer Report - Alan R Parrish |
| 14 Jul 2018 | Reviewed | Reviewer Report - Nirmala D Sirisena |
| 22 Aug 2018 | Reviewed | Reviewer Report - Eikan Mishima |
| 20 Sep 2018 | Author responded | Author comments - Wenjun Yang |
| Resubmission - Version 2 | ||
| 20 Sep 2018 | Submitted | Manuscript version 2 |
| 21 Sep 2018 | Reviewed | Reviewer Report - Eikan Mishima |
| 25 Sep 2018 | Reviewed | Reviewer Report - Nirmala D Sirisena |
| 30 Oct 2018 | Author responded | Author comments - Wenjun Yang |
| Resubmission - Version 3 | ||
| 30 Oct 2018 | Submitted | Manuscript version 3 |
| 22 Nov 2018 | Author responded | Author comments - Wenjun Yang |
| Resubmission - Version 4 | ||
| 22 Nov 2018 | Submitted | Manuscript version 4 |
| 28 Nov 2018 | Author responded | Author comments - Wenjun Yang |
| Resubmission - Version 5 | ||
| 28 Nov 2018 | Submitted | Manuscript version 5 |
| Publishing | ||
| 29 Nov 2018 | Editorially accepted | |
| 17 Dec 2018 | Article published | 10.1186/s12882-018-1163-3 |
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