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Peer Review reports

From: Phenotype, origin and estimated prevalence of a common long QT syndrome mutation: a clinical, genealogical and molecular genetics study including Swedish R518X/KCNQ1families

Original Submission
12 Nov 2013 Submitted Original manuscript
28 Dec 2013 Reviewed Reviewer Report - Bo Gregers Winkel
27 Jan 2014 Reviewed Reviewer Report - Knut Erik Berge
4 Feb 2014 Author responded Author comments - Annika Winbo
Resubmission - Version 2
4 Feb 2014 Submitted Manuscript version 2
Publishing
14 Feb 2014 Editorially accepted
19 Feb 2014 Article published 10.1186/1471-2261-14-22

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