Intronic PRRT2 mutation generates novel splice acceptor site and causes paroxysmal kinesigenic dyskinesia with infantile convulsions (PKD/IC) in a three generation family

Peer Review reports

Original Submission
20 Nov 2015	Submitted	Original manuscript
9 Feb 2016	Reviewed	Reviewer Report - Andreas Puschmann
10 Feb 2016	Reviewed	Reviewer Report - Susanne Schneider
18 Feb 2016	Author responded	Author comments - Axel Weber
Resubmission - Version 2
18 Feb 2016	Submitted	Manuscript version 2
Publishing
26 Feb 2016	Editorially accepted
3 Mar 2016	Article published	10.1186/s12881-016-0281-7

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