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Peer Review reports

From: A Chinese case of Nakajo–Nishimura syndrome with novel compound heterozygous mutations of the PSMB8 gene

Original Submission
6 Nov 2019 Submitted Original manuscript
19 Nov 2019 Author responded Author comments - Jia Tao
7 Jan 2020 Reviewed Reviewer Report - Venkateshwari Ananthapur
17 Jan 2020 Reviewed Reviewer Report - Prabhakar S Kedar
15 Feb 2020 Author responded Author comments - Jia Tao
Resubmission - Version 2
19 Nov 2019 Submitted Manuscript version 2
5 Mar 2020 Author responded Author comments - Jia Tao
Resubmission - Version 3
5 Mar 2020 Submitted Manuscript version 3
10 Mar 2020 Author responded Author comments - Jia Tao
Resubmission - Version 4
10 Mar 2020 Submitted Manuscript version 4
19 Mar 2020 Author responded Author comments - Jia Tao
Resubmission - Version 5
19 Mar 2020 Submitted Manuscript version 5
24 Mar 2020 Author responded Author comments - Tao Jia
Resubmission - Version 6
24 Mar 2020 Submitted Manuscript version 6
5 May 2020 Author responded Author comments - Tao Jia
Resubmission - Version 7
5 May 2020 Submitted Manuscript version 7
10 May 2020 Author responded Author comments - Tao Jia
Resubmission - Version 8
10 May 2020 Submitted Manuscript version 8
Publishing
24 May 2020 Editorially accepted
8 Jun 2020 Article published 10.1186/s12881-020-01060-8

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