A novel AP4M1 mutation in autosomal recessive cerebral palsy syndrome and clinical expansion of AP-4 deficiency

Peer Review reports

Original Submission
30 Jun 2014	Submitted	Original manuscript
22 Jul 2014	Author responded	Author comments - Niklas Dahl
Resubmission - Version 2
22 Jul 2014	Submitted	Manuscript version 2
2 Aug 2014	Reviewed	Reviewer Report - Annick Raas-Rothschild
8 Aug 2014	Reviewed	Reviewer Report - Kerstin Kutsche
Resubmission - Version 3
	Submitted	Manuscript version 3
12 Sep 2014	Author responded	Author comments - Niklas Dahl
Resubmission - Version 4
12 Sep 2014	Submitted	Manuscript version 4
26 Sep 2014	Reviewed	Reviewer Report - Kerstin Kutsche
10 Oct 2014	Reviewed	Reviewer Report - Annick Raas-Rothschild
16 Oct 2014	Author responded	Author comments - Niklas Dahl
Resubmission - Version 5
16 Oct 2014	Submitted	Manuscript version 5
31 Oct 2014	Author responded	Author comments - Niklas Dahl
Resubmission - Version 6
31 Oct 2014	Submitted	Manuscript version 6
13 Nov 2014	Author responded	Author comments - Niklas Dahl
Resubmission - Version 7
13 Nov 2014	Submitted	Manuscript version 7
1 Dec 2014	Author responded	Author comments - Niklas Dahl
Resubmission - Version 8
1 Dec 2014	Submitted	Manuscript version 8
Publishing
3 Dec 2014	Editorially accepted
14 Dec 2014	Article published	10.1186/s12881-014-0133-2

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