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Peer Review reports

From: Case report of homozygous deletion involving the first coding exons of GCNT2 isoforms A and B and part of the upstream region of TFAP2A in congenital cataract

Original Submission
23 Apr 2016 Submitted Original manuscript
Author responded Author comments
Reviewed Reviewer Report
Resubmission - Version 2
Submitted Manuscript version 2
Publishing
28 Jul 2016 Editorially accepted
8 Sep 2016 Article published 10.1186/s12881-016-0316-0

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