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Peer Review reports

From: Novel intragenic deletion within the FXN gene in a patient with typical phenotype of Friedreich ataxia: may be more prevalent than we think?

Original Submission
5 Dec 2022 Submitted Original manuscript
25 Jan 2023 Reviewed Reviewer Report
23 Feb 2023 Reviewed Reviewer Report - Suran Nethisinghe
3 Jun 2023 Author responded Author comments - Cinthia Aguilera
Resubmission - Version 2
3 Jun 2023 Submitted Manuscript version 2
5 Jun 2023 Author responded Author comments - Cinthia Aguilera
Resubmission - Version 3
5 Jun 2023 Submitted Manuscript version 3
20 Jun 2023 Reviewed Reviewer Report
28 Jun 2023 Reviewed Reviewer Report - Suran Nethisinghe
13 Jul 2023 Author responded Author comments - Cinthia Aguilera
Resubmission - Version 4
13 Jul 2023 Submitted Manuscript version 4
24 Aug 2023 Author responded Author comments - Cinthia Aguilera
Resubmission - Version 5
24 Aug 2023 Submitted Manuscript version 5
31 Aug 2023 Author responded Author comments - Cinthia Aguilera
Resubmission - Version 6
31 Aug 2023 Submitted Manuscript version 6
18 Sep 2023 Reviewed Reviewer Report
10 Oct 2023 Reviewed Reviewer Report - Suran Nethisinghe
15 Nov 2023 Author responded Author comments - Cinthia Aguilera
Resubmission - Version 7
15 Nov 2023 Submitted Manuscript version 7
Publishing
18 Nov 2023 Editorially accepted
1 Dec 2023 Article published 10.1186/s12920-023-01743-0

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