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Peer Review reports

From: A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population

Original Submission
20 May 2012 Submitted Original manuscript
22 May 2012 Author responded Author comments - Sebastien Levesque
Resubmission - Version 2
22 May 2012 Submitted Manuscript version 2
11 Jun 2012 Reviewed Reviewer Report - William Rizzo
27 Jun 2012 Reviewed Reviewer Report - Robert Steiner
23 Jul 2012 Author responded Author comments - Sebastien Levesque
Resubmission - Version 3
23 Jul 2012 Submitted Manuscript version 3
Publishing
8 Aug 2012 Editorially accepted
15 Aug 2012 Article published 10.1186/1471-2350-13-72

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