Clinical exome sequencing identifies two novel mutations of the SCN1A and SCN2A genes in Moroccan patients with epilepsy: a case series

Peer Review reports

Original Submission
29 Mar 2019	Submitted	Original manuscript
19 Jun 2019	Reviewed	Reviewer Report - Arun Karthikeyan
26 Jun 2019	Reviewed	Reviewer Report - Adriano Alberti
8 Jul 2019	Author responded	Author comments - Maryem Sahli
Resubmission - Version 2
8 Jul 2019	Submitted	Manuscript version 2
Publishing
17 Jul 2019	Editorially accepted
23 Aug 2019	Article published	10.1186/s13256-019-2203-8

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