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Peer Review reports

From: Concurrent OPA1 mutation and chromosome 3q deletion leading to Behr syndrome: a case report

Original Submission
25 Feb 2020 Submitted Original manuscript
9 May 2020 Author responded Author comments - Wei Shuzhang
Resubmission - Version 2
9 May 2020 Submitted Manuscript version 2
27 Jun 2020 Reviewed Reviewer Report - Dominique Bonneau
20 Jul 2020 Reviewed Reviewer Report
15 Aug 2020 Author responded Author comments - Wei Shuzhang
Resubmission - Version 3
15 Aug 2020 Submitted Manuscript version 3
Publishing
20 Aug 2020 Editorially accepted
3 Sep 2020 Article published 10.1186/s12887-020-02309-0

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