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Peer Review reports

From: Whole-exome sequencing reveals a rare missense variant in DTNA in an Iranian pedigree with early-onset atrial fibrillation

Original Submission
27 Oct 2021 Submitted Original manuscript
9 Dec 2021 Reviewed Reviewer Report
14 Dec 2021 Reviewed Reviewer Report - J Alexander Kharlamov
1 Jan 2022 Author responded Author comments - Majid Haghjoo
Resubmission - Version 2
1 Jan 2022 Submitted Manuscript version 2
11 Jan 2022 Author responded Author comments - Majid Haghjoo
Resubmission - Version 3
11 Jan 2022 Submitted Manuscript version 3
23 Jan 2022 Reviewed Reviewer Report - J Alexander Kharlamov
28 Jan 2022 Reviewed Reviewer Report
Resubmission - Version 4
Submitted Manuscript version 4
Publishing
31 Jan 2022 Editorially accepted
11 Feb 2022 Article published 10.1186/s12872-022-02485-0

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BMC Cardiovascular Disorders

ISSN: 1471-2261

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