Peer review reports
From: Association of a rare NOTCH4 coding variant with systemic sclerosis: a family-based whole exome sequencing study
| Original Submission |
| 30 Jul 2016 |
Submitted |
Original manuscript
|
|
Author responded |
Author comments
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| Resubmission - Version 2 |
|
Submitted |
Manuscript version 2
|
|
Author responded |
Author comments
|
| Resubmission - Version 3 |
|
Submitted |
Manuscript version 3
|
| Publishing |
| 1 Nov 2016 |
Editorially accepted |
|
| 9 Nov 2016 |
Article published |
10.1186/s12891-016-1320-4
|
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