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Peer Review reports

From: A novel 1.38-kb deletion combined with a single nucleotide variant in KIAA0586 as a cause of Joubert syndrome

Original Submission
30 Aug 2022 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
10 Oct 2022 Reviewed Reviewer Report
18 Oct 2022 Reviewed Reviewer Report
9 Nov 2022 Author responded Author comments - Minna Luo
Resubmission - Version 3
9 Nov 2022 Submitted Manuscript version 3
11 Nov 2022 Author responded Author comments - Minna Luo
Resubmission - Version 4
11 Nov 2022 Submitted Manuscript version 4
22 Nov 2022 Author responded Author comments - Minna Luo
Resubmission - Version 5
22 Nov 2022 Submitted Manuscript version 5
20 Dec 2022 Reviewed Reviewer Report
2 Jan 2023 Reviewed Reviewer Report
6 Jan 2023 Author responded Author comments - Minna Luo
Resubmission - Version 6
6 Jan 2023 Submitted Manuscript version 6
9 Jan 2023 Author responded Author comments - Minna Luo
Resubmission - Version 7
9 Jan 2023 Submitted Manuscript version 7
Publishing
10 Jan 2023 Editorially accepted
12 Jan 2023 Article published 10.1186/s12920-023-01438-6

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