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Peer Review reports

From: Mutations in NFKB2 and potential genetic heterogeneity in patients with DAVID syndrome, having variable endocrine and immune deficiencies

Original Submission
26 Sep 2014 Submitted Original manuscript
13 Oct 2014 Reviewed Reviewer Report - Claudio Pignata
6 Nov 2014 Reviewed Reviewer Report - Raffaele Badolato
25 Nov 2014 Author responded Author comments - Mark Samuels
Resubmission - Version 2
25 Nov 2014 Submitted Manuscript version 2
10 Dec 2014 Author responded Author comments - Mark Samuels
Resubmission - Version 3
10 Dec 2014 Submitted Manuscript version 3
Publishing
11 Dec 2014 Editorially accepted
19 Dec 2014 Article published 10.1186/s12881-014-0139-9

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