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Peer Review reports

From: Diagnosis delay a family of Galloway-Mowat Syndrome caused by a classical splicing mutation of Lage3

Original Submission
22 Apr 2022 Submitted Original manuscript
6 May 2022 Reviewed Reviewer Report
22 May 2022 Reviewed Reviewer Report
7 Aug 2022 Author responded Author comments - Yan Chen
Resubmission - Version 2
7 Aug 2022 Submitted Manuscript version 2
31 Oct 2022 Author responded Author comments - Yan Chen
Resubmission - Version 3
31 Oct 2022 Submitted Manuscript version 3
Publishing
5 Nov 2022 Editorially accepted
8 Feb 2023 Article published 10.1186/s12882-022-03000-5

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