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Peer Review reports

From: The mutational spectrum of hunter syndrome reveals correlation between biochemical and clinical profiles in Tunisian patients

Original Submission
25 Aug 2019 Submitted Original manuscript
25 Sep 2019 Author responded Author comments - Latifa Chkioua
9 Oct 2019 Author responded Author comments - Latifa Chkioua
Resubmission - Version 2
25 Sep 2019 Submitted Manuscript version 2
25 Oct 2019 Reviewed Reviewer Report - Mohammad Abdi
2 Nov 2019 Reviewed Reviewer Report - Xijie Yu
6 Nov 2019 Reviewed Reviewer Report - Alla Semyachkina
12 Nov 2019 Reviewed Reviewer Report - sabika firasat
11 Dec 2019 Author responded Author comments - Latifa Chkioua
Resubmission - Version 3
11 Dec 2019 Submitted Manuscript version 3
26 Dec 2019 Reviewed Reviewer Report - Mohammad Abdi
6 Jan 2020 Reviewed Reviewer Report - sabika firasat
4 Feb 2020 Author responded Author comments - Latifa Chkioua
Resubmission - Version 4
4 Feb 2020 Submitted Manuscript version 4
24 Feb 2020 Author responded Author comments - Latifa Chkioua
Resubmission - Version 5
24 Feb 2020 Submitted Manuscript version 5
28 Feb 2020 Author responded Author comments - Latifa Chkioua
Resubmission - Version 6
28 Feb 2020 Submitted Manuscript version 6
4 Mar 2020 Author responded Author comments - Latifa Chkioua
Resubmission - Version 7
4 Mar 2020 Submitted Manuscript version 7
5 Mar 2020 Author responded Author comments - Latifa Chkioua
Resubmission - Version 8
5 Mar 2020 Submitted Manuscript version 8
7 May 2020 Author responded Author comments - Latifa Chkioua
Resubmission - Version 9
7 May 2020 Submitted Manuscript version 9
Publishing
14 May 2020 Editorially accepted
24 May 2020 Article published 10.1186/s12881-020-01051-9

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