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Peer Review reports

From: A likely pathogenic POLD1 variant associated with mandibular hypoplasia, deafness, progeroid features, and lipodystrophy syndrome in a Chinese patient

Original Submission
2 Jul 2022 Submitted Original manuscript
10 Aug 2022 Reviewed Reviewer Report
12 Aug 2022 Reviewed Reviewer Report
3 Sep 2022 Author responded Author comments - Wei Lu
Resubmission - Version 2
3 Sep 2022 Submitted Manuscript version 2
14 Sep 2022 Author responded Author comments - Wei Lu
Resubmission - Version 3
14 Sep 2022 Submitted Manuscript version 3
20 Sep 2022 Author responded Author comments - Wei Lu
Resubmission - Version 4
20 Sep 2022 Submitted Manuscript version 4
Publishing
5 Oct 2022 Editorially accepted
21 Oct 2022 Article published 10.1186/s12920-022-01374-x

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