Peer Review reports
From: Truncating ARL6IP1 variant as the genetic cause of fatal complicated hereditary spastic paraplegia
| Original Submission | ||
|---|---|---|
| 3 Mar 2019 | Submitted | Original manuscript |
| 31 Mar 2019 | Author responded | Author comments - salma majid |
| Resubmission - Version 2 | ||
| 31 Mar 2019 | Submitted | Manuscript version 2 |
| 8 Apr 2019 | Reviewed | Reviewer Report - Mohammad Faghihi |
| 1 May 2019 | Reviewed | Reviewer Report - Milica Keckarevic Markovic |
| 3 Jun 2019 | Author responded | Author comments - salma majid |
| Resubmission - Version 3 | ||
| 3 Jun 2019 | Submitted | Manuscript version 3 |
| 17 Jun 2019 | Author responded | Author comments - salma majid |
| Resubmission - Version 4 | ||
| 17 Jun 2019 | Submitted | Manuscript version 4 |
| Publishing | ||
| 19 Jun 2019 | Editorially accepted | |
| 4 Jul 2019 | Article published | 10.1186/s12881-019-0851-6 |
You can find further information about peer review here.