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Peer Review reports

From: Next-generation sequencing for D47N mutation in Cx50 analysis associated with autosomal dominant congenital cataract in a six-generation Chinese family

Original Submission
22 Sep 2016 Submitted Original manuscript
8 Oct 2016 Reviewed Reviewer Report - Lyubomyr Lytvynchuk
18 Nov 2016 Reviewed Reviewer Report - Alan Shiels
15 Dec 2016 Author responded Author comments - chao shen
Resubmission - Version 2
15 Dec 2016 Submitted Manuscript version 2
4 Feb 2017 Author responded Author comments - chao shen
Resubmission - Version 3
4 Feb 2017 Submitted Manuscript version 3
13 Feb 2017 Author responded Author comments - chao shen
Resubmission - Version 4
13 Feb 2017 Submitted Manuscript version 4
22 Mar 2017 Author responded Author comments - chao shen
Resubmission - Version 5
22 Mar 2017 Submitted Manuscript version 5
20 Apr 2017 Author responded Author comments - chao shen
Resubmission - Version 6
20 Apr 2017 Submitted Manuscript version 6
5 May 2017 Author responded Author comments - chao shen
Resubmission - Version 7
5 May 2017 Submitted Manuscript version 7
Publishing
15 May 2017 Editorially accepted
19 May 2017 Article published 10.1186/s12886-017-0476-5

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