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Peer Review reports

From: A novel missense mutation in the CLCN7 gene linked to benign autosomal dominant osteopetrosis: a case series

Original Submission
21 Apr 2012 Submitted Original manuscript
Resubmission - Version 2
Submitted Manuscript version 2
28 Apr 2012 Author responded Author comments - Beston F. Nore
Resubmission - Version 3
28 Apr 2012 Submitted Manuscript version 3
28 Apr 2012 Author responded Author comments - Beston F. Nore
Resubmission - Version 4
28 Apr 2012 Submitted Manuscript version 4
1 Jun 2012 Reviewed Reviewer Report - Anna Villa
13 Jul 2012 Reviewed Reviewer Report - Elena Bliznetz
16 Aug 2012 Author responded Author comments - Beston F. Nore
Resubmission - Version 5
16 Aug 2012 Submitted Manuscript version 5
16 Aug 2012 Author responded Author comments - Beston F. Nore
Resubmission - Version 6
16 Aug 2012 Submitted Manuscript version 6
29 Aug 2012 Reviewed Reviewer Report - Anna Villa
27 Sep 2012 Author responded Author comments - Beston F. Nore
Resubmission - Version 7
27 Sep 2012 Submitted Manuscript version 7
17 Oct 2012 Author responded Author comments - Beston F. Nore
Resubmission - Version 8
17 Oct 2012 Submitted Manuscript version 8
19 Oct 2012 Author responded Author comments - Beston F. Nore
Resubmission - Version 9
19 Oct 2012 Submitted Manuscript version 9
21 Oct 2012 Author responded Author comments - Beston F. Nore
Resubmission - Version 10
21 Oct 2012 Submitted Manuscript version 10
8 Nov 2012 Author responded Author comments - Beston F. Nore
Resubmission - Version 11
8 Nov 2012 Submitted Manuscript version 11
10 Nov 2012 Author responded Author comments - Beston F. Nore
Resubmission - Version 12
10 Nov 2012 Submitted Manuscript version 12
Publishing
13 Nov 2012 Editorially accepted
9 Jan 2013 Article published 10.1186/1752-1947-7-7

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