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Peer Review reports

From: A rare co-occurrence of duchenne muscular dystrophy, congenital adrenal hypoplasia and glycerol kinase deficiency due to Xp21 contiguous gene deletion syndrome: case report

Original Submission
24 Dec 2020 Submitted Original manuscript
14 Mar 2021 Reviewed Reviewer Report
16 Mar 2021 Reviewed Reviewer Report - Vijaya Sarathi
6 Apr 2021 Author responded Author comments - Asanka Rathnasri
Resubmission - Version 2
6 Apr 2021 Submitted Manuscript version 2
10 Jun 2021 Reviewed Reviewer Report - Vijaya Sarathi
23 Jun 2021 Reviewed Reviewer Report
1 Jul 2021 Author responded Author comments - Asanka Rathnasri
Resubmission - Version 3
1 Jul 2021 Submitted Manuscript version 3
24 Sep 2021 Author responded Author comments - Asanka Rathnasri
Resubmission - Version 4
24 Sep 2021 Submitted Manuscript version 4
12 Oct 2021 Author responded Author comments - Asanka Rathnasri
Resubmission - Version 5
12 Oct 2021 Submitted Manuscript version 5
Publishing
15 Oct 2021 Editorially accepted
24 Oct 2021 Article published 10.1186/s12902-021-00876-6

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