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Peer Review reports

From: Clinical and Genetic Study on a Chinese Patient with Infantile Onset Epileptic Encephalopathy carrying a PPP3CA Null Variant: a case report

Original Submission
6 Dec 2019 Submitted Original manuscript
19 May 2020 Author responded Author comments - Sai Yang
7 Apr 2020 Reviewed Reviewer Report - Livia Pisciotta
28 Apr 2020 Reviewed Reviewer Report
Resubmission - Version 2
19 May 2020 Submitted Manuscript version 2
15 Jun 2020 Author responded Author comments - Sai Yang
4 Jun 2020 Reviewed Reviewer Report
Resubmission - Version 3
15 Jun 2020 Submitted Manuscript version 3
Publishing
17 Jun 2020 Editorially accepted
27 Jun 2020 Article published 10.1186/s12887-020-02213-7

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