A novel SLC6A8 mutation associated with intellectual disabilities in a Chinese family exhibiting creatine transporter deficiency: case report

Peer Review reports

Original Submission
26 Jul 2018	Submitted	Original manuscript
12 Sep 2018	Reviewed	Reviewer Report - Halil Ibrahim Aydin
17 Sep 2018	Reviewed	Reviewer Report - Christopher Wassif
17 Oct 2018	Author responded	Author comments - Qin Wang
Resubmission - Version 2
17 Oct 2018	Submitted	Manuscript version 2
Publishing
22 Oct 2018	Editorially accepted
6 Nov 2018	Article published	10.1186/s12881-018-0707-5

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