Peer review reports
From: Chinese families with autosomal recessive hereditary spastic paraplegia caused by mutations in SPG11
Original Submission | ||
---|---|---|
10 Oct 2019 | Submitted | Original manuscript |
3 Nov 2019 | Reviewed | Reviewer Report - Varvara Andreevna Kadnikova |
6 Nov 2019 | Reviewed | Reviewer Report - Quiao Wei |
12 Dec 2019 | Author responded | Author comments - Xueping Chen |
Resubmission - Version 2 | ||
12 Dec 2019 | Submitted | Manuscript version 2 |
18 Dec 2019 | Author responded | Author comments - Xueping Chen |
Resubmission - Version 3 | ||
18 Dec 2019 | Submitted | Manuscript version 3 |
26 Dec 2019 | Author responded | Author comments - Xueping Chen |
Resubmission - Version 4 | ||
26 Dec 2019 | Submitted | Manuscript version 4 |
Publishing | ||
29 Dec 2019 | Editorially accepted | |
3 Jan 2020 | Article published | 10.1186/s12883-019-1593-y |