Open Access Pre-publication history

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

Catalina Dussaillant, Valentina Serrano, Alberto Maiz, Susana Eyheramendy, Luis Rodrigo Cataldo, Matías Chavez, Susan V Smalley, Marcela Fuentes, Attilio Rigotti, Lorena Rubio, Carlos F Lagos, José Alfredo Martinez and José Luis Santos*

BMC Medical Genetics 2012, 13:106  doi:10.1186/1471-2350-13-106

Pre-publication versions of this article and reviewers' reports

Original Submission - Version 1 Manuscript 06 Jan 2012
Reviewer's Report Angelo Baldassare Cefalu 20 Mar 2012
Reviewer's Report sybil charriere 23 Mar 2012
Resubmission - Version 2 Manuscript Author's comment 31 Jul 2012
Reviewer's Report sybil charriere 14 Aug 2012
Resubmission - Version 3 Manuscript Author's comment 31 Aug 2012
Resubmission - Version 4 Manuscript Author's comment 22 Oct 2012
Editorial acceptance 23 Oct 2012
Published 15 Nov 2012