Skip to main content

Peer Review reports

From: A novel nonsense mutation in WNK1/HSN2 associated with sensory neuropathy and limb destruction in four siblings of a large Iranian pedigree

Original Submission
14 Jun 2018 Submitted Original manuscript
12 Aug 2018 Reviewed Reviewer Report - Efterpi Pavlidou
31 Aug 2018 Reviewed Reviewer Report - Hiroaki Adachi
1 Oct 2018 Reviewed Reviewer Report - Ingo Kurth
1 Oct 2018 Reviewed Reviewer Report - Andrzej Kochanski
23 Oct 2018 Author responded Author comments - Behrouz Rahmani
Resubmission - Version 2
23 Oct 2018 Submitted Manuscript version 2
14 Nov 2018 Author responded Author comments - Behrouz Rahmani
Resubmission - Version 3
14 Nov 2018 Submitted Manuscript version 3
Publishing
19 Nov 2018 Editorially accepted
29 Nov 2018 Article published 10.1186/s12883-018-1201-6

You can find further information about peer review here.

Back to article page