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Peer Review reports

From: APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family

Original Submission
6 Jan 2012 Submitted Original manuscript
20 Mar 2012 Reviewed Reviewer Report - Angelo Baldassare Cefalu
23 Mar 2012 Reviewed Reviewer Report - sybil charriere
31 Jul 2012 Author responded Author comments - Catalina Dussaillant
Resubmission - Version 2
31 Jul 2012 Submitted Manuscript version 2
14 Aug 2012 Reviewed Reviewer Report - sybil charriere
31 Aug 2012 Author responded Author comments - Catalina Dussaillant
Resubmission - Version 3
31 Aug 2012 Submitted Manuscript version 3
22 Oct 2012 Author responded Author comments - Catalina Dussaillant
Resubmission - Version 4
22 Oct 2012 Submitted Manuscript version 4
Publishing
23 Oct 2012 Editorially accepted
15 Nov 2012 Article published 10.1186/1471-2350-13-106

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