This article has Open Peer Review reports available.
A de novo CTNNB1 nonsense mutation associated with syndromic atypical hyperekplexia, microcephaly and intellectual disability: a case report
© Winczewska-Wiktor et al. 2016
Received: 30 September 2015
Accepted: 26 February 2016
Published: 12 March 2016
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting email@example.com.
|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|
|26 Feb 2016||Editorially accepted|
|12 Mar 2016||Article published||10.1186/s12883-016-0554-y|
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