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Peer Review reports

From: A novel compound heterozygous BEST1 gene mutation in two siblings causing autosomal recessive bestrophinopathy

Original Submission
3 Feb 2022 Submitted Original manuscript
22 Mar 2022 Reviewed Reviewer Report - Santasree Banerjee
9 Jun 2022 Reviewed Reviewer Report
23 Jul 2022 Author responded Author comments - Obaid Imtiyazul Haque
Resubmission - Version 2
23 Jul 2022 Submitted Manuscript version 2
3 Aug 2022 Author responded Author comments - Obaid Imtiyazul Haque
Resubmission - Version 3
3 Aug 2022 Submitted Manuscript version 3
8 Aug 2022 Author responded Author comments - Obaid Imtiyazul Haque
Resubmission - Version 4
8 Aug 2022 Submitted Manuscript version 4
22 Aug 2022 Reviewed Reviewer Report - Santasree Banerjee
20 Sep 2022 Reviewed Reviewer Report
5 Oct 2022 Author responded Author comments - Obaid Imtiyazul Haque
Resubmission - Version 5
5 Oct 2022 Submitted Manuscript version 5
7 Oct 2022 Author responded Author comments - Obaid Imtiyazul Haque
Resubmission - Version 6
7 Oct 2022 Submitted Manuscript version 6
8 Nov 2022 Reviewed Reviewer Report
18 Nov 2022 Author responded Author comments - Obaid Imtiyazul Haque
Resubmission - Version 7
18 Nov 2022 Submitted Manuscript version 7
Publishing
23 Nov 2022 Editorially accepted
16 Dec 2022 Article published 10.1186/s12886-022-02703-5

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