This article has Open Peer Review reports available.
Novel loss-of-function PRRT2mutation causes paroxysmal kinesigenic dyskinesia in a Han Chinese family
- Zhisong Ji†1,
- Quanxi Su†2,
- Lingling Hu1,
- Qi Yang1,
- Cuixian Liu1,
- Jun Xiong1 and
- Fu Xiong1Email author
© Ji et al.; licensee BioMed Central Ltd. 2014
Received: 31 March 2014
Accepted: 7 July 2014
Published: 16 July 2014
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting firstname.lastname@example.org.
|31 Mar 2014||Submitted||Original manuscript|
|8 Apr 2014||Reviewed||Reviewer Report - Jianfeng Xiao|
|9 Apr 2014||Reviewed||Reviewer Report - Peter Hedera|
|23 May 2014||Author responded||Author comments - zhisong ji|
|Resubmission - Version 2|
|23 May 2014||Submitted||Manuscript version 2|
|7 Jun 2014||Reviewed||Reviewer Report - Jianfeng Xiao|
|29 Jun 2014||Author responded||Author comments - zhisong ji|
|Resubmission - Version 3|
|29 Jun 2014||Submitted||Manuscript version 3|
|4 Jul 2014||Author responded||Author comments - zhisong ji|
|Resubmission - Version 4|
|4 Jul 2014||Submitted||Manuscript version 4|
|7 Jul 2014||Editorially accepted|
|16 Jul 2014||Article published||10.1186/1471-2377-14-146|
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