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 |