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Peer Review reports

From: POLG1 p.R722H mutation associated with multiple mtDNA deletions and a neurological phenotype

Original Submission
29 Jul 2009 Submitted Original manuscript
6 Aug 2009 Author responded Author comments - Tuomas Komulainen
Resubmission - Version 2
6 Aug 2009 Submitted Manuscript version 2
7 Sep 2009 Reviewed Reviewer Report - Rita Horvath
9 Sep 2009 Reviewed Reviewer Report - Nereo Bresolin
19 Sep 2009 Reviewed Reviewer Report - Michio Hirano
31 Jan 2010 Author responded Author comments - Tuomas Komulainen
Resubmission - Version 3
31 Jan 2010 Submitted Manuscript version 3
24 Feb 2010 Reviewed Reviewer Report - Michio Hirano
4 Mar 2010 Reviewed Reviewer Report - Nereo Bresolin
Resubmission - Version 4
Submitted Manuscript version 4
Resubmission - Version 5
Submitted Manuscript version 5
15 Apr 2010 Author responded Author comments - Tuomas Komulainen
Resubmission - Version 6
15 Apr 2010 Submitted Manuscript version 6
Resubmission - Version 7
Submitted Manuscript version 7
22 Apr 2010 Author responded Author comments - Tuomas Komulainen
Resubmission - Version 8
22 Apr 2010 Submitted Manuscript version 8
Publishing
3 May 2010 Editorially accepted
3 May 2010 Article published 10.1186/1471-2377-10-29

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