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Peer Review reports

From: SPG9A with the new occurrence of an ALDH18A1 mutation in a CMT1A family with PMP22 duplication: case report

Original Submission
20 Nov 2020 Submitted Original manuscript
19 Jan 2021 Author responded Author comments - Kishin Koh
17 Dec 2020 Reviewed Reviewer Report - Zhihua Yang
11 Jan 2021 Reviewed Reviewer Report
Resubmission - Version 2
19 Jan 2021 Submitted Manuscript version 2
29 Jan 2021 Author responded Author comments - Kishin Koh
Resubmission - Version 3
29 Jan 2021 Submitted Manuscript version 3
Publishing
2 Feb 2021 Editorially accepted
11 Feb 2021 Article published 10.1186/s12883-021-02087-x

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