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 |
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