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Peer Review reports

From: A homozygous AHI1 gene mutation (p.Thr304AsnfsX6) in a consanguineous Moroccan family with Joubert syndrome: a case report

Original Submission
18 Dec 2014 Submitted Original manuscript
Author responded Author comments
Resubmission - Version 2
Submitted Manuscript version 2
Resubmission - Version 3
Submitted Manuscript version 3
Resubmission - Version 4
Submitted Manuscript version 4
Resubmission - Version 5
Submitted Manuscript version 5
Author responded Author comments
Reviewed Reviewer Report
Resubmission - Version 6
Submitted Manuscript version 6
Reviewed Reviewer Report
Resubmission - Version 7
Submitted Manuscript version 7
Publishing
8 Oct 2015 Editorially accepted
5 Nov 2015 Article published 10.1186/s13256-015-0732-3

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