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Peer Review reports

From: A unique homozygous WRAP53 Arg298Trp mutation underlies dyskeratosis congenita in a Chinese Han family

Original Submission
20 Sep 2017 Submitted Original manuscript
3 Nov 2017 Reviewed Reviewer Report - Owen Smith
6 Nov 2017 Reviewed Reviewer Report - Judy Wong
16 Nov 2017 Reviewed Reviewer Report - Amanda J. Walne
18 Nov 2017 Reviewed Reviewer Report - Manop Pithukpakorn
4 Jan 2018 Author responded Author comments - Yinqi Shao
Resubmission - Version 2
4 Jan 2018 Submitted Manuscript version 2
7 Jan 2018 Reviewed Reviewer Report - Judy Wong
15 Jan 2018 Reviewed Reviewer Report - Amanda J. Walne
17 Jan 2018 Reviewed Reviewer Report - Manop Pithukpakorn
30 Jan 2018 Author responded Author comments - Yinqi Shao
Resubmission - Version 3
30 Jan 2018 Submitted Manuscript version 3
31 Jan 2018 Reviewed Reviewer Report - Judy Wong
12 Feb 2018 Reviewed Reviewer Report - Amanda J. Walne
16 Feb 2018 Author responded Author comments - Yinqi Shao
Resubmission - Version 4
16 Feb 2018 Submitted Manuscript version 4
Publishing
23 Feb 2018 Editorially accepted
7 Mar 2018 Article published 10.1186/s12881-018-0549-1

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