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Peer Review reports

From: Novel pathogenic OCRL mutations and genotype–phenotype analysis of Chinese children affected by oculocerebrorenal syndrome: two cases and a literature review

Original Submission
28 Dec 2020 Submitted Original manuscript
24 Mar 2021 Reviewed Reviewer Report
6 Apr 2021 Reviewed Reviewer Report
4 May 2021 Author responded Author comments - Yu Zhang
Resubmission - Version 2
4 May 2021 Submitted Manuscript version 2
11 May 2021 Author responded Author comments - Yu Zhang
Resubmission - Version 3
11 May 2021 Submitted Manuscript version 3
29 May 2021 Author responded Author comments - Yu Zhang
Resubmission - Version 4
29 May 2021 Submitted Manuscript version 4
27 Jun 2021 Author responded Author comments - Yu Zhang
Resubmission - Version 5
27 Jun 2021 Submitted Manuscript version 5
9 Jul 2021 Author responded Author comments - Yu Zhang
Resubmission - Version 6
9 Jul 2021 Submitted Manuscript version 6
17 Aug 2021 Author responded Author comments - Yu Zhang
Resubmission - Version 7
17 Aug 2021 Submitted Manuscript version 7
23 Aug 2021 Author responded Author comments - Yu Zhang
Resubmission - Version 8
23 Aug 2021 Submitted Manuscript version 8
26 Aug 2021 Author responded Author comments - Yu Zhang
Resubmission - Version 9
26 Aug 2021 Submitted Manuscript version 9
Publishing
27 Aug 2021 Editorially accepted
6 Sep 2021 Article published 10.1186/s12920-021-01069-9

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