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

Peer Review reports

Original Submission
20 Aug 2012	Submitted	Original manuscript
Resubmission - Version 2
	Submitted	Manuscript version 2
29 Jan 2013	Reviewed	Reviewer Report - NiChung Lee
4 Feb 2013	Author responded	Author comments - Monika Obara-Moszynska
Resubmission - Version 3
4 Feb 2013	Submitted	Manuscript version 3
6 Feb 2013	Reviewed	Reviewer Report - NiChung Lee
Resubmission - Version 4
	Submitted	Manuscript version 4
Publishing
12 Feb 2013	Editorially accepted
20 Feb 2013	Article published	10.1186/1471-2431-13-27

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