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Peer Review reports

From: MFN2 point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT families

Original Submission
5 Oct 2009 Submitted Original manuscript
22 Oct 2009 Reviewed Reviewer Report - Henry Houlden
13 Nov 2009 Reviewed Reviewer Report - Moritz Meins
23 Nov 2009 Reviewed Reviewer Report - Peter De Jonghe
9 Dec 2009 Author responded Author comments - Geir Julius Braathen
Resubmission - Version 2
9 Dec 2009 Submitted Manuscript version 2
14 Dec 2009 Reviewed Reviewer Report - Henry Houlden
4 Jan 2010 Reviewed Reviewer Report - Moritz Meins
24 Feb 2010 Author responded Author comments - Geir Julius Braathen
Resubmission - Version 3
24 Feb 2010 Submitted Manuscript version 3
11 Mar 2010 Author responded Author comments - Geir Julius Braathen
Resubmission - Version 4
11 Mar 2010 Submitted Manuscript version 4
Resubmission - Version 5
Submitted Manuscript version 5
23 Mar 2010 Author responded Author comments - Geir Julius Braathen
Resubmission - Version 6
23 Mar 2010 Submitted Manuscript version 6
Publishing
29 Mar 2010 Editorially accepted
29 Mar 2010 Article published 10.1186/1471-2350-11-48

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