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Peer Review reports

From: Molecular analysis of a consanguineous Iranian polycystic kidney disease family identifies a PKD2 mutation that aids diagnostics

Original Submission
24 May 2013 Submitted Original manuscript
5 Jul 2013 Author responded Author comments - Peter Harris
Resubmission - Version 2
5 Jul 2013 Submitted Manuscript version 2
10 Aug 2013 Reviewed Reviewer Report - Richard Sandford
10 Aug 2013 Reviewed Reviewer Report - Roser Torra
27 Aug 2013 Author responded Author comments - Peter Harris
Resubmission - Version 3
27 Aug 2013 Submitted Manuscript version 3
Publishing
4 Sep 2013 Editorially accepted
8 Sep 2013 Article published 10.1186/1471-2369-14-190

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