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Peer Review reports

From: Novel nonsense mutation p. Gln264Ter in the ANK1 confirms causative role for hereditary spherocytosis: a case report

Original Submission
4 Jul 2020 Submitted Original manuscript
23 Jul 2020 Author responded Author comments - Senmao Chai
Resubmission - Version 2
23 Jul 2020 Submitted Manuscript version 2
24 Sep 2020 Reviewed Reviewer Report
2 Oct 2020 Reviewed Reviewer Report - Venkateshwari Ananthapur
13 Oct 2020 Author responded Author comments - Senmao Chai
Resubmission - Version 3
13 Oct 2020 Submitted Manuscript version 3
28 Oct 2020 Author responded Author comments - Senmao Chai
Resubmission - Version 4
28 Oct 2020 Submitted Manuscript version 4
Publishing
29 Oct 2020 Editorially accepted
13 Nov 2020 Article published 10.1186/s12881-020-01161-4

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