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Peer Review reports

From: Heterozygous p.Asp50Asn mutation in the GJB2 gene in two Cameroonian patients with keratitis-ichthyosis-deafness (KID) syndrome

Original Submission
21 Feb 2013 Submitted Original manuscript
12 Mar 2013 Reviewed Reviewer Report - Ralf Birkenhäger
2 Apr 2013 Reviewed Reviewer Report - Regie Lyn Santos-Cortez
19 Apr 2013 Author responded Author comments - Ambroise Wonkam
Resubmission - Version 2
19 Apr 2013 Submitted Manuscript version 2
26 Jun 2013 Reviewed Reviewer Report - Regie Lyn Santos-Cortez
1 Jul 2013 Author responded Author comments - Ambroise Wonkam
Resubmission - Version 3
1 Jul 2013 Submitted Manuscript version 3
Publishing
7 Aug 2013 Editorially accepted
7 Aug 2013 Article published 10.1186/1471-2350-14-81

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