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Peer Review reports

From: A novel homozygous missense substitution p.Thr313Ile in the PDE6B gene underlies autosomal recessive retinitis pigmentosa in a consanguineous Pakistani family

Original Submission
7 Aug 2022 Submitted Original manuscript
19 Sep 2022 Reviewed Reviewer Report - Chitaranjan Mishra
16 Oct 2022 Reviewed Reviewer Report
23 Oct 2022 Author responded Author comments - Atta Ur Rehman
Resubmission - Version 2
23 Oct 2022 Submitted Manuscript version 2
16 Nov 2022 Reviewed Reviewer Report
12 Jan 2023 Author responded Author comments - Atta Ur Rehman
Resubmission - Version 3
12 Jan 2023 Submitted Manuscript version 3
24 Jan 2023 Author responded Author comments - Atta Ur Rehman
Resubmission - Version 4
24 Jan 2023 Submitted Manuscript version 4
6 Feb 2023 Author responded Author comments - Atta Ur Rehman
Resubmission - Version 5
6 Feb 2023 Submitted Manuscript version 5
23 Feb 2023 Author responded Author comments - Atta Ur Rehman
Resubmission - Version 6
23 Feb 2023 Submitted Manuscript version 6
Publishing
7 Mar 2023 Editorially accepted
23 Mar 2023 Article published 10.1186/s12886-023-02845-0

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