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Peer Review reports

From: Mild cognitive impairment in novel SPG11 mutation-related sporadic hereditary spastic paraplegia with thin corpus callosum: case series

Original Submission
17 Aug 2020 Submitted Original manuscript
26 Aug 2020 Author responded Author comments - Chuan Li
Resubmission - Version 2
26 Aug 2020 Submitted Manuscript version 2
5 Oct 2020 Reviewed Reviewer Report
11 Oct 2020 Reviewed Reviewer Report - Kishore Kumar
10 Nov 2020 Author responded Author comments - Chuan Li
Resubmission - Version 3
10 Nov 2020 Submitted Manuscript version 3
21 Dec 2020 Author responded Author comments - Chuan Li
Resubmission - Version 4
21 Dec 2020 Submitted Manuscript version 4
23 Dec 2020 Author responded Author comments - Chuan Li
Resubmission - Version 5
23 Dec 2020 Submitted Manuscript version 5
Publishing
29 Dec 2020 Editorially accepted
11 Jan 2021 Article published 10.1186/s12883-020-02040-4

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