APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family
© Dussaillant et al.; licensee BioMed Central Ltd. 2012
Received: 6 January 2012
Accepted: 23 October 2012
Published: 15 November 2012
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting firstname.lastname@example.org.
|6 Jan 2012||Submitted||Original manuscript|
|Resubmission - Version 2|
|Submitted||Manuscript version 2|
|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 3|
|31 Jul 2012||Submitted||Manuscript version 3|
|14 Aug 2012||Reviewed||Reviewer Report - sybil charriere|
|31 Aug 2012||Author responded||Author comments - Catalina Dussaillant|
|Resubmission - Version 4|
|31 Aug 2012||Submitted||Manuscript version 4|
|22 Oct 2012||Author responded||Author comments - Catalina Dussaillant|
|Resubmission - Version 5|
|22 Oct 2012||Submitted||Manuscript version 5|
|23 Oct 2012||Editorially accepted|
|15 Nov 2012||Article published||10.1186/1471-2350-13-106|
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