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Peer Review reports

From: Connexin 26 ( GJB2 ) mutation in an Argentinean patient with keratitis-ichthyosis-deafness (KID) syndrome: a case report

Original Submission
2 Sep 2015 Submitted Original manuscript
6 Dec 2015 Reviewed Reviewer Report - Nathalie Jonca
7 Dec 2015 Reviewed Reviewer Report - Qiaoli Li
18 Jan 2016 Author responded Author comments - Viviana K Dalamon
Resubmission - Version 2
18 Jan 2016 Submitted Manuscript version 2
18 Feb 2016 Author responded Author comments - Viviana K Dalamon
Resubmission - Version 3
18 Feb 2016 Submitted Manuscript version 3
Publishing
22 Apr 2016 Editorially accepted
4 May 2016 Article published 10.1186/s12881-016-0298-y

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