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Peer Review reports

From: Molecular diagnosis of hereditary inclusion body myopathy by linkage analysis and identification of a novel splice site mutation in GNE

Original Submission
23 Dec 2010 Submitted Original manuscript
11 Jan 2011 Author responded Author comments - Steven Boyden
Resubmission - Version 2
11 Jan 2011 Submitted Manuscript version 2
10 Mar 2011 Reviewed Reviewer Report - Iris Eisenberg - Loebl
11 Mar 2011 Reviewed Reviewer Report - May Christine Malicdan
23 Mar 2011 Reviewed Reviewer Report - Sabine Krause
20 Apr 2011 Author responded Author comments - Steven Boyden
Resubmission - Version 3
20 Apr 2011 Submitted Manuscript version 3
6 May 2011 Reviewed Reviewer Report - Iris Eisenberg - Loebl
6 May 2011 Reviewed Reviewer Report - Sabine Krause
7 May 2011 Reviewed Reviewer Report - May Christine Malicdan
23 May 2011 Author responded Author comments - Steven Boyden
Resubmission - Version 4
23 May 2011 Submitted Manuscript version 4
6 Jun 2011 Reviewed Reviewer Report - May Christine Malicdan
21 Jun 2011 Author responded Author comments - Steven Boyden
Resubmission - Version 5
21 Jun 2011 Submitted Manuscript version 5
Publishing
28 Jun 2011 Editorially accepted
28 Jun 2011 Article published 10.1186/1471-2350-12-87

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