Skip to main content

Peer Review reports

From: A Chinese patient with 11β-hydroxylase deficiency due to novel compound heterozygous mutation in CYP11B1 gene: a case report

Original Submission
2 Nov 2017 Submitted Original manuscript
20 Nov 2017 Author responded Author comments - Xianxian Yuan
Resubmission - Version 2
20 Nov 2017 Submitted Manuscript version 2
1 Feb 2018 Reviewed Reviewer Report - Maja Stojiljkovic
21 May 2018 Reviewed Reviewer Report - CLAUDIO ELIAS Kater
27 May 2018 Reviewed Reviewer Report - Mirjana Kocova
7 Jul 2018 Author responded Author comments - Xianxian Yuan
Resubmission - Version 3
7 Jul 2018 Submitted Manuscript version 3
17 Jul 2018 Reviewed Reviewer Report - Mirjana Kocova
18 Jul 2018 Reviewed Reviewer Report - Maja Stojiljkovic
6 Aug 2018 Reviewed Reviewer Report - CLAUDIO ELIAS Kater
3 Sep 2018 Author responded Author comments - Xianxian Yuan
Resubmission - Version 4
3 Sep 2018 Submitted Manuscript version 4
10 Sep 2018 Author responded Author comments - Xianxian Yuan
Resubmission - Version 5
10 Sep 2018 Submitted Manuscript version 5
Publishing
13 Sep 2018 Editorially accepted
21 Sep 2018 Article published 10.1186/s12902-018-0295-6

You can find further information about peer review here.

Back to article page