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Peer Review reports

From: Identification of compound mutations of SLC12A3 gene in a Chinese pedigree with Gitelman syndrome exhibiting Bartter syndrome-liked phenotypes

Original Submission
21 Mar 2020 Submitted Original manuscript
28 Mar 2020 Author responded Author comments - Dong Bingzi
Resubmission - Version 2
28 Mar 2020 Submitted Manuscript version 2
20 May 2020 Author responded Author comments - Dong Bingzi
3 Apr 2020 Reviewed Reviewer Report
23 Apr 2020 Reviewed Reviewer Report
Resubmission - Version 3
20 May 2020 Submitted Manuscript version 3
21 Jun 2020 Author responded Author comments - Dong Bingzi
9 Jun 2020 Reviewed Reviewer Report
18 Jun 2020 Reviewed Reviewer Report
Resubmission - Version 4
21 Jun 2020 Submitted Manuscript version 4
10 Jul 2020 Author responded Author comments - Bingzi Dong
22 Jun 2020 Reviewed Reviewer Report
Resubmission - Version 5
10 Jul 2020 Submitted Manuscript version 5
24 Jul 2020 Author responded Author comments - Bingzi Dong
Resubmission - Version 6
24 Jul 2020 Submitted Manuscript version 6
Publishing
30 Jul 2020 Editorially accepted
5 Aug 2020 Article published 10.1186/s12882-020-01996-2

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