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Peer Review reports

From: Mutations in Danish patients with long QT syndrome and the identification of a large founder family with p.F29L in KCNH2

Original Submission
4 Oct 2013 Submitted Original manuscript
1 Nov 2013 Reviewed Reviewer Report - Elijah Behr
26 Nov 2013 Reviewed Reviewer Report - britt maria beckmann
10 Feb 2014 Author responded Author comments - Michael Christiansen
Resubmission - Version 2
10 Feb 2014 Submitted Manuscript version 2
Publishing
18 Feb 2014 Editorially accepted
7 Mar 2014 Article published 10.1186/1471-2350-15-31

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