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Peer Review reports

From: A heterozygous mutation in the CCDC88C gene likely causes early-onset pure hereditary spastic paraplegia: a case report

Original Submission
15 Oct 2020 Submitted Original manuscript
12 Dec 2020 Reviewed Reviewer Report
20 Dec 2020 Reviewed Reviewer Report
21 Dec 2020 Reviewed Reviewer Report
2 Jan 2021 Author responded Author comments - Ashraf Yahia
Resubmission - Version 2
2 Jan 2021 Submitted Manuscript version 2
9 Feb 2021 Author responded Author comments - Ashraf Yahia
Resubmission - Version 3
9 Feb 2021 Submitted Manuscript version 3
Publishing
12 Feb 2021 Editorially accepted
18 Feb 2021 Article published 10.1186/s12883-021-02113-y

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