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Peer Review reports

From: Exome sequencing identifies a mutation in the ACTN2 gene in a family with idiopathic ventricular fibrillation, left ventricular noncompaction, and sudden death

Original Submission
30 Jan 2014 Submitted Original manuscript
1 Feb 2014 Author responded Author comments - Christopher Semsarian
Resubmission - Version 2
1 Feb 2014 Submitted Manuscript version 2
17 Apr 2014 Reviewed Reviewer Report - Andrew Davis
21 Apr 2014 Reviewed Reviewer Report - michael gollob
21 Apr 2014 Reviewed Reviewer Report - Patrice Bouvagnet
21 May 2014 Author responded Author comments - Christopher Semsarian
Resubmission - Version 3
21 May 2014 Submitted Manuscript version 3
Publishing
12 Aug 2014 Editorially accepted
16 Sep 2014 Article published 10.1186/s12881-014-0099-0

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BMC Medical Genetics

ISSN: 1471-2350

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