Skip to main content

Peer Review reports

From: Exome sequencing circumvents missing clinical data and identifies a BSCL2 mutation in congenital lipodystrophy

Original Submission
13 Mar 2014 Submitted Original manuscript
30 Apr 2014 Reviewed Reviewer Report - Sandro Banfi
20 May 2014 Reviewed Reviewer Report - Massimiliano Rossi
2 Jun 2014 Author responded Author comments - Joakim Klar
Resubmission - Version 2
2 Jun 2014 Submitted Manuscript version 2
3 Jun 2014 Author responded Author comments - Joakim Klar
Resubmission - Version 3
3 Jun 2014 Submitted Manuscript version 3
9 Jun 2014 Author responded Author comments - Joakim Klar
Resubmission - Version 4
9 Jun 2014 Submitted Manuscript version 4
Publishing
10 Jun 2014 Editorially accepted
24 Jun 2014 Article published 10.1186/1471-2350-15-71

You can find further information about peer review here.

Back to article page