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Peer Review reports

From: Novel heterozygous compound TRMT5 mutations associated with combined oxidative phosphorylation deficiency 26 in a Chinese family: a case report

Original Submission
9 Aug 2021 Submitted Original manuscript
5 Oct 2021 Reviewed Reviewer Report - Carla Cristina de Morais
10 Oct 2021 Reviewed Reviewer Report
10 Oct 2021 Reviewed Reviewer Report
25 Nov 2021 Author responded Author comments - Shuiyan Wu
Resubmission - Version 2
25 Nov 2021 Submitted Manuscript version 2
18 Dec 2021 Reviewed Reviewer Report
19 Dec 2021 Reviewed Reviewer Report
27 Dec 2021 Author responded Author comments - Shuiyan Wu
Resubmission - Version 3
27 Dec 2021 Submitted Manuscript version 3
26 Jan 2022 Author responded Author comments - Shuiyan Wu
Resubmission - Version 4
26 Jan 2022 Submitted Manuscript version 4
Publishing
27 Jan 2022 Editorially accepted
2 Feb 2022 Article published 10.1186/s12887-022-03138-z

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