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Peer Review reports

From: Two patients with Knobloch syndrome due to mutation in COL8A1 gene: case report and review of the literature

Original Submission
5 Feb 2023 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
Resubmission - Version 3
Submitted Manuscript version 3
7 Sep 2023 Reviewed Reviewer Report
4 Oct 2023 Reviewed Reviewer Report
20 Nov 2023 Reviewed Reviewer Report
4 Dec 2023 Author responded Author comments - TÜLİN ÖĞREDEN
Resubmission - Version 4
4 Dec 2023 Submitted Manuscript version 4
30 Dec 2023 Author responded Author comments - TÜLİN ÖĞREDEN
Resubmission - Version 5
30 Dec 2023 Submitted Manuscript version 5
9 Jan 2024 Author responded Author comments - TÜLİN ÖĞREDEN
Resubmission - Version 6
9 Jan 2024 Submitted Manuscript version 6
16 Jan 2024 Reviewed Reviewer Report
18 Jan 2024 Reviewed Reviewer Report
31 Jan 2024 Author responded Author comments - TÜLİN ÖĞREDEN
Resubmission - Version 7
31 Jan 2024 Submitted Manuscript version 7
26 Feb 2024 Author responded Author comments - TÜLİN ÖĞREDEN
Resubmission - Version 8
26 Feb 2024 Submitted Manuscript version 8
4 Mar 2024 Author responded Author comments - TÜLİN ÖĞREDEN
Resubmission - Version 9
4 Mar 2024 Submitted Manuscript version 9
17 Mar 2024 Reviewed Reviewer Report
25 Mar 2024 Author responded Author comments - TÜLİN ÖĞREDEN
Resubmission - Version 10
25 Mar 2024 Submitted Manuscript version 10
Publishing
29 Mar 2024 Editorially accepted
4 Apr 2024 Article published 10.1186/s12886-024-03418-5

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