Analysis of 31-year-old patient with SYNGAP1 gene defect points to importance of variants in broader splice regions and reveals developmental trajectory of SYNGAP1-associated phenotype: case report

Peer Review reports

Original Submission
23 Jan 2017	Submitted	Original manuscript
19 Apr 2017	Reviewed	Reviewer Report - Raquel Rabionet
20 Apr 2017	Reviewed	Reviewer Report - Singh Rajender
10 May 2017	Author responded	Author comments - Darina Prchalova
Resubmission - Version 2
10 May 2017	Submitted	Manuscript version 2
19 May 2017	Author responded	Author comments - Darina Prchalova
Resubmission - Version 3
19 May 2017	Submitted	Manuscript version 3
Publishing
22 May 2017	Editorially accepted
2 Jun 2017	Article published	10.1186/s12881-017-0425-4

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