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Peer Review reports

From: A novel pathogenic variant in the carnitine transporter gene, SLC22A5, in association with metabolic carnitine deficiency and cardiomyopathy features

Original Submission
26 Apr 2023 Submitted Original manuscript
5 Jul 2023 Reviewed Reviewer Report - Mahmut Cerkez Ergoren
17 Jul 2023 Reviewed Reviewer Report
13 Sep 2023 Reviewed Reviewer Report
14 Oct 2023 Author responded Author comments - Samira Kalayinia
Resubmission - Version 2
14 Oct 2023 Submitted Manuscript version 2
15 Oct 2023 Author responded Author comments - Samira Kalayinia
Resubmission - Version 3
15 Oct 2023 Submitted Manuscript version 3
15 Oct 2023 Author responded Author comments - Samira Kalayinia
Resubmission - Version 4
15 Oct 2023 Submitted Manuscript version 4
31 Oct 2023 Reviewed Reviewer Report
15 Nov 2023 Reviewed Reviewer Report
21 Nov 2023 Author responded Author comments - Samira Kalayinia
Resubmission - Version 5
21 Nov 2023 Submitted Manuscript version 5
29 Nov 2023 Author responded Author comments - Samira Kalayinia
Resubmission - Version 6
29 Nov 2023 Submitted Manuscript version 6
Publishing
15 Dec 2023 Editorially accepted
2 Jan 2024 Article published 10.1186/s12872-023-03676-z

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