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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