This article has Open Peer Review reports available.
Clinical and molecular features of an infant patient affected by Leigh Disease associated to m.14459G > A mitochondrial DNA mutation: a case report
© Ronchi et al; licensee BioMed Central Ltd. 2011
Received: 7 March 2011
Accepted: 12 July 2011
Published: 12 July 2011
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting email@example.com.
|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|
|12 Jul 2011||Editorially accepted|
|12 Jul 2011||Article published||10.1186/1471-2377-11-85|
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