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Peer Review reports

From: Novel GUCY2D mutation causes phenotypic variability of Leber congenital amaurosis in a large kindred

Original Submission
21 Jan 2016 Submitted Original manuscript
6 Jun 2016 Reviewed Reviewer Report - Kinga Bujakowska
10 Jun 2016 Reviewed Reviewer Report - Birgit Lorenz
15 Jul 2016 Author responded Author comments - Libe Gradstein
Resubmission - Version 2
15 Jul 2016 Submitted Manuscript version 2
Publishing
21 Jul 2016 Editorially accepted
30 Jul 2016 Article published 10.1186/s12881-016-0314-2

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