A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: a late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment
© Obara-Moszynska et al.; licensee BioMed Central Ltd. 2013
Received: 20 August 2012
Accepted: 12 February 2013
Published: 20 February 2013
Open Peer Review reports
Pre-publication versions of this article and author comments to reviewers are available by contacting firstname.lastname@example.org.
|20 Aug 2012||Submitted||Original manuscript|
|Resubmission - Version 2|
|Submitted||Manuscript version 2|
|Resubmission - Version 3|
|Submitted||Manuscript version 3|
|29 Jan 2013||Reviewed||Reviewer Report - NiChung Lee|
|4 Feb 2013||Author responded||Author comments - Monika Obara-Moszynska|
|Resubmission - Version 4|
|4 Feb 2013||Submitted||Manuscript version 4|
|6 Feb 2013||Reviewed||Reviewer Report - NiChung Lee|
|Resubmission - Version 5|
|Submitted||Manuscript version 5|
|12 Feb 2013||Editorially accepted|
|20 Feb 2013||Article published||10.1186/1471-2431-13-27|
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