Open Access Highly Accessed Pre-publication history

Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing

Eva-Lena Stattin*, Ida Maria Boström, Annika Winbo, Kristina Cederquist, Jenni Jonasson, Björn-Anders Jonsson, Ulla-Britt Diamant, Steen M Jensen, Annika Rydberg and Anna Norberg

BMC Cardiovascular Disorders 2012, 12:95  doi:10.1186/1471-2261-12-95

Pre-publication versions of this article and reviewers' reports

Original Submission - Version 1 Manuscript 28 Jun 2012
Resubmission - Version 2 Manuscript Author's comment 29 Jun 2012
Reviewer's Report David Tester 21 Aug 2012
Reviewer's Report Pier Lambiase 31 Aug 2012
Resubmission - Version 3 Manuscript Author's comment 19 Sep 2012
Reviewer's Report David Tester 21 Sep 2012
Reviewer's Report Pier Lambiase 08 Oct 2012
Editorial acceptance 10 Oct 2012
Published 25 Oct 2012