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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
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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