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Peer Review reports

From: Heterozygous deletion of SCN2A and SCN3A in a patient with autism spectrum disorder and Tourette syndrome: a case report

Original Submission
28 Nov 2017 Submitted Original manuscript
8 Feb 2018 Reviewed Reviewer Report - Mohammed Uddin
10 Apr 2018 Reviewed Reviewer Report - Marco A. Grados
10 May 2018 Author responded Author comments - Kathrin Nickel
Resubmission - Version 2
10 May 2018 Submitted Manuscript version 2
15 May 2018 Reviewed Reviewer Report - Mohammed Uddin
Resubmission - Version 3
Submitted Manuscript version 3
Publishing
19 Jul 2018 Editorially accepted
2 Aug 2018 Article published 10.1186/s12888-018-1822-8

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