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Peer Review reports

From: Identification of a novel heterozygous SPTB mutation by whole genome sequencing in a Chinese patient with hereditary spherocytosis and atrial septal defect: a case report

Original Submission
7 Sep 2020 Submitted Original manuscript
9 Nov 2020 Reviewed Reviewer Report
11 Dec 2020 Reviewed Reviewer Report
15 Dec 2020 Reviewed Reviewer Report
13 Jan 2021 Author responded Author comments - Zhanhui Du
Resubmission - Version 2
13 Jan 2021 Submitted Manuscript version 2
8 Feb 2021 Reviewed Reviewer Report
9 Feb 2021 Reviewed Reviewer Report
10 Feb 2021 Reviewed Reviewer Report
19 Feb 2021 Author responded Author comments - Zhanhui Du
Resubmission - Version 3
19 Feb 2021 Submitted Manuscript version 3
22 Feb 2021 Reviewed Reviewer Report
18 Mar 2021 Reviewed Reviewer Report
20 May 2021 Author responded Author comments - Zhanhui Du
Resubmission - Version 4
20 May 2021 Submitted Manuscript version 4
24 May 2021 Reviewed Reviewer Report
8 Jun 2021 Reviewed Reviewer Report
11 Jun 2021 Author responded Author comments - Zhanhui Du
Resubmission - Version 5
11 Jun 2021 Submitted Manuscript version 5
Publishing
14 Jun 2021 Editorially accepted
28 Jun 2021 Article published 10.1186/s12887-021-02771-4

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