Skip to main content

Peer Review reports

From: A de novo CTNNB1 nonsense mutation associated with syndromic atypical hyperekplexia, microcephaly and intellectual disability: a case report

Original Submission
30 Sep 2015 Submitted Original manuscript
5 Nov 2015 Reviewed Reviewer Report - Fakhri Kallabi
14 Nov 2015 Reviewed Reviewer Report - Daojun Hong
14 Dec 2016 Author responded Author comments - Anna Winczewska-Wiktor
Resubmission - Version 2
14 Dec 2016 Submitted Manuscript version 2
17 Jan 2016 Author responded Author comments - Anna Winczewska-Wiktor
Resubmission - Version 3
17 Jan 2016 Submitted Manuscript version 3
Publishing
26 Feb 2016 Editorially accepted
12 Mar 2016 Article published 10.1186/s12883-016-0554-y

You can find further information about peer review here.

Back to article page