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Peer Review reports

From: A novel mutation of the RPGRIP1L gene in a Chinese boy with Joubert syndrome with oculorenal involvement

Original Submission
3 Feb 2023 Submitted Original manuscript
21 Feb 2023 Reviewed Reviewer Report - Wen-Xiong Chen
12 Apr 2023 Reviewed Reviewer Report
19 Oct 2023 Author responded Author comments - Shuzhen Sun
Resubmission - Version 2
19 Oct 2023 Submitted Manuscript version 2
23 Oct 2023 Author responded Author comments - Shuzhen Sun
Resubmission - Version 3
23 Oct 2023 Submitted Manuscript version 3
3 Nov 2023 Reviewed Reviewer Report
9 Nov 2023 Reviewed Reviewer Report - Wen-Xiong Chen
Resubmission - Version 4
Submitted Manuscript version 4
Publishing
10 Nov 2023 Editorially accepted
23 Nov 2023 Article published 10.1186/s12887-023-04415-1

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