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Peer Review reports

From: Attenuated clinical and osteoclastic phenotypes of Paget’s disease of bone linked to the p.Pro392Leu/SQSTM1 mutation by a rare variant in the DOCK6 gene

Original Submission
17 Oct 2021 Submitted Original manuscript
28 Dec 2021 Reviewed Reviewer Report
30 Dec 2021 Reviewed Reviewer Report - Ali Sazci
30 Jan 2022 Author responded Author comments - Laëtitia Michou
Resubmission - Version 2
30 Jan 2022 Submitted Manuscript version 2
18 Feb 2022 Reviewed Reviewer Report
Resubmission - Version 3
Submitted Manuscript version 3
Publishing
24 Feb 2022 Editorially accepted
3 Mar 2022 Article published 10.1186/s12920-022-01198-9

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BMC Medical Genomics

ISSN: 1755-8794

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