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Peer Review reports

From: Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups

Original Submission
21 Nov 2019 Submitted Original manuscript
24 Jan 2020 Reviewed Reviewer Report - Hermann Girschick
3 Feb 2020 Reviewed Reviewer Report - Sigrun Ruth Hofmann
18 Mar 2020 Author responded Author comments - Gunter Aßmann
17 Apr 2020 Author responded Author comments - Gunter Aßmann
Resubmission - Version 2
18 Mar 2020 Submitted Manuscript version 2
22 Apr 2020 Author responded Author comments - Gunter Aßmann
Resubmission - Version 3
22 Apr 2020 Submitted Manuscript version 3
23 Apr 2020 Author responded Author comments - Gunter Aßmann
Resubmission - Version 4
23 Apr 2020 Submitted Manuscript version 4
25 Apr 2020 Author responded Author comments - Gunter Aßmann
Resubmission - Version 5
25 Apr 2020 Submitted Manuscript version 5
Publishing
28 Apr 2020 Editorially accepted
12 May 2020 Article published 10.1186/s12881-020-01037-7

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