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Peer Review reports

From: First molecular study in Lebanese patients with Cockayne syndrome and report of a novel mutation in ERCC8 gene

Original Submission
3 May 2018 Submitted Original manuscript
19 Jun 2018 Reviewed Reviewer Report - Nadege Calmels
10 Jul 2018 Reviewed Reviewer Report - Elena Botta
14 Aug 2018 Author responded Author comments - Alain Chebly
Resubmission - Version 2
14 Aug 2018 Submitted Manuscript version 2
30 Aug 2018 Author responded Author comments - Alain Cheblys
Resubmission - Version 3
30 Aug 2018 Submitted Manuscript version 3
Publishing
31 Aug 2018 Editorially accepted
10 Sep 2018 Article published 10.1186/s12881-018-0677-7

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