Skip to main content

Peer Review reports

From: A child with genetic FN1 mutation in the absence of classic glomerulopathy with fibronectin deposits(GFND) findings on biopsy

Original Submission
24 Dec 2021 Submitted Original manuscript
5 Mar 2022 Author responded Author comments - Xiao-qing Yang
Resubmission - Version 2
5 Mar 2022 Submitted Manuscript version 2
16 Mar 2022 Reviewed Reviewer Report
27 Mar 2022 Reviewed Reviewer Report
29 Mar 2022 Reviewed Reviewer Report
19 May 2022 Author responded Author comments - Xiao-qing Yang
Resubmission - Version 3
19 May 2022 Submitted Manuscript version 3
20 Jun 2022 Author responded Author comments - Xiao-qing Yang
Resubmission - Version 4
20 Jun 2022 Submitted Manuscript version 4
28 Jun 2022 Author responded Author comments - Xiao-qing Yang
Resubmission - Version 5
28 Jun 2022 Submitted Manuscript version 5
Publishing
3 Jul 2022 Editorially accepted
14 Jul 2022 Article published 10.1186/s12882-022-02872-x

You can find further information about peer review here.

Back to article page