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Peer Review reports

From: Dent-2 disease with a Bartter-like phenotype caused by the Asp631Glu mutation in the OCRL gene

Original Submission
31 Mar 2021 Submitted Original manuscript
5 Sep 2021 Reviewed Reviewer Report
7 Sep 2021 Reviewed Reviewer Report
9 Sep 2021 Author responded Author comments - Eleni Drosataki
Resubmission - Version 2
9 Sep 2021 Submitted Manuscript version 2
29 Nov 2021 Reviewed Reviewer Report
Resubmission - Version 3
Submitted Manuscript version 3
Publishing
4 May 2022 Editorially accepted
12 May 2022 Article published 10.1186/s12882-022-02812-9

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