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Peer Review reports

From: Novel compound heterozygous mutations of MTHFR Gene in a Chinese family with homocystinuria due to MTHFR deficiency

Original Submission
1 Jul 2022 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
Resubmission - Version 3
Submitted Manuscript version 3
27 Sep 2022 Reviewed Reviewer Report
2 Oct 2022 Reviewed Reviewer Report
17 Oct 2022 Author responded Author comments - Xinwen Zhang
Resubmission - Version 4
17 Oct 2022 Submitted Manuscript version 4
22 Oct 2022 Author responded Author comments - Xinwen Zhang
Resubmission - Version 5
22 Oct 2022 Submitted Manuscript version 5
29 Oct 2022 Author responded Author comments - Xinwen Zhang
Resubmission - Version 6
29 Oct 2022 Submitted Manuscript version 6
6 Nov 2022 Reviewed Reviewer Report
11 Nov 2022 Author responded Author comments - Xinwen Zhang
Resubmission - Version 7
11 Nov 2022 Submitted Manuscript version 7
18 Nov 2022 Reviewed Reviewer Report
30 Nov 2022 Reviewed Reviewer Report
Resubmission - Version 8
Submitted Manuscript version 8
Publishing
5 Dec 2022 Editorially accepted
25 Dec 2022 Article published 10.1186/s12920-022-01408-4

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