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Peer Review reports

From: Recurrent NUS1 canonical splice donor site mutation in two unrelated individuals with epilepsy, myoclonus, ataxia and scoliosis - a case report

Original Submission
28 May 2019 Submitted Original manuscript
17 Jul 2019 Reviewed Reviewer Report - Yasukiyo Araki
26 Aug 2019 Reviewed Reviewer Report - Sho Yano
2 Sep 2019 Author responded Author comments - Kouhei Den
Resubmission - Version 2
2 Sep 2019 Submitted Manuscript version 2
4 Sep 2019 Reviewed Reviewer Report - Sho Yano
18 Sep 2019 Reviewed Reviewer Report - Yasukiyo Araki
1 Oct 2019 Author responded Author comments - Kouhei Den
Resubmission - Version 3
1 Oct 2019 Submitted Manuscript version 3
Publishing
2 Oct 2019 Editorially accepted
27 Oct 2019 Article published 10.1186/s12883-019-1489-x

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