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Peer Review reports

From: Selected AGXT gene mutations analysis provides a genetic diagnosis in 28% of Tunisian patients with primary hyperoxaluria

Original Submission
11 Oct 2010 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
1 Dec 2010 Reviewed Reviewer Report - Marion Coulter-Mackie
6 Dec 2010 Reviewed Reviewer Report - Gill Rumsby
9 Dec 2010 Reviewed Reviewer Report - antonio amoroso
Resubmission - Version 3
Submitted Manuscript version 3
25 Jan 2011 Author responded Author comments - asma omezzine
Resubmission - Version 4
25 Jan 2011 Submitted Manuscript version 4
10 Feb 2011 Reviewed Reviewer Report - Gill Rumsby
15 Mar 2011 Reviewed Reviewer Report - Marion Coulter-Mackie
25 Mar 2011 Author responded Author comments - asma omezzine
Resubmission - Version 5
25 Mar 2011 Submitted Manuscript version 5
6 Apr 2011 Author responded Author comments - asma omezzine
Resubmission - Version 6
6 Apr 2011 Submitted Manuscript version 6
Resubmission - Version 7
Submitted Manuscript version 7
16 May 2011 Author responded Author comments - asma omezzine
Resubmission - Version 8
16 May 2011 Submitted Manuscript version 8
Resubmission - Version 9
Submitted Manuscript version 9
21 May 2011 Author responded Author comments - asma omezzine
Resubmission - Version 10
21 May 2011 Submitted Manuscript version 10
Publishing
25 May 2011 Editorially accepted
25 May 2011 Article published 10.1186/1471-2369-12-25

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