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Peer Review reports

From: Clinical manifestation and genetic findings in three boys with low molecular Weight Proteinuria - three case reports for exploring Dent Disease and Fanconi syndrome

Original Submission
8 Apr 2020 Submitted Original manuscript
10 May 2020 Reviewed Reviewer Report
2 Jun 2020 Reviewed Reviewer Report
2 Jul 2020 Author responded Author comments - Nan Duan
Resubmission - Version 2
2 Jul 2020 Submitted Manuscript version 2
26 Jul 2020 Reviewed Reviewer Report
3 Aug 2020 Reviewed Reviewer Report
1 Sep 2020 Author responded Author comments - Nan Duan
Resubmission - Version 3
1 Sep 2020 Submitted Manuscript version 3
7 Sep 2020 Reviewed Reviewer Report
28 Sep 2020 Reviewed Reviewer Report
12 Oct 2020 Reviewed Reviewer Report
1 Dec 2020 Author responded Author comments - Nan Duan
Resubmission - Version 4
1 Dec 2020 Submitted Manuscript version 4
14 Dec 2020 Reviewed Reviewer Report
16 Dec 2020 Reviewed Reviewer Report
19 Dec 2020 Author responded Author comments - Nan Duan
Resubmission - Version 5
19 Dec 2020 Submitted Manuscript version 5
Publishing
23 Dec 2020 Editorially accepted
11 Jan 2021 Article published 10.1186/s12882-020-02225-6

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