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Peer Review reports

From: Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G > A mitochondrial DNA mutation: a case report

Original Submission
7 Mar 2011 Submitted Original manuscript
18 Apr 2011 Reviewed Reviewer Report - Monique Ryan
27 Apr 2011 Reviewed Reviewer Report - Eppie Yiu
25 May 2011 Author responded Author comments - Giacomo Comi
Resubmission - Version 2
25 May 2011 Submitted Manuscript version 2
3 Jul 2011 Reviewed Reviewer Report - Eppie Yiu
9 Jul 2011 Author responded Author comments - Giacomo Comi
Resubmission - Version 3
9 Jul 2011 Submitted Manuscript version 3
Publishing
12 Jul 2011 Editorially accepted
12 Jul 2011 Article published 10.1186/1471-2377-11-85

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