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Peer Review reports

From: Epilepsy as the symptom of a spinocerebellar ataxia 13 in a patient presenting with a mutation in the KCNC3 gene

Original Submission
19 Apr 2023 Submitted Original manuscript
6 May 2023 Reviewed Reviewer Report - Wen-Xiong Chen
10 May 2023 Reviewed Reviewer Report
13 Jun 2023 Author responded Author comments - Shao Li
22 Jun 2023 Reviewed Reviewer Report - Wen-Xiong Chen
Resubmission - Version 2
13 Jun 2023 Submitted Manuscript version 2
Publishing
23 Jun 2023 Editorially accepted
26 Jun 2023 Article published 10.1186/s12883-023-03304-5

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