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Peer Review reports

From: Rare hereditary nonspherocytic hemolytic anemia caused by a novel homozygous mutation, c.301C > A, (Q101K), in the AK1 gene in an Indian family

Original Submission
12 Jan 2021 Submitted Original manuscript
29 Jan 2021 Author responded Author comments - Rashmi Dongerdiye
Resubmission - Version 2
29 Jan 2021 Submitted Manuscript version 2
12 Feb 2021 Reviewed Reviewer Report
15 Mar 2021 Reviewed Reviewer Report
15 Apr 2021 Author responded Author comments - Rashmi Dongerdiye
Resubmission - Version 3
15 Apr 2021 Submitted Manuscript version 3
4 May 2021 Reviewed Reviewer Report
12 May 2021 Author responded Author comments - Rashmi Dongerdiye
Resubmission - Version 4
12 May 2021 Submitted Manuscript version 4
21 May 2021 Author responded Author comments - Rashmi Dongerdiye
Resubmission - Version 5
21 May 2021 Submitted Manuscript version 5
28 May 2021 Author responded Author comments - Rashmi Dongerdiye
Resubmission - Version 6
28 May 2021 Submitted Manuscript version 6
4 Jun 2021 Author responded Author comments - Rashmi Dongerdiye
Resubmission - Version 7
4 Jun 2021 Submitted Manuscript version 7
10 Jun 2021 Author responded Author comments - Rashmi Dongerdiye
Resubmission - Version 8
10 Jun 2021 Submitted Manuscript version 8
1 Jul 2021 Author responded Author comments - Rashmi Dongerdiye
Resubmission - Version 9
1 Jul 2021 Submitted Manuscript version 9
16 Jul 2021 Author responded Author comments - Rashmi Dongerdiye
Resubmission - Version 10
16 Jul 2021 Submitted Manuscript version 10
20 Jul 2021 Author responded Author comments - Rashmi Dongerdiye
Resubmission - Version 11
20 Jul 2021 Submitted Manuscript version 11
Publishing
21 Jul 2021 Editorially accepted
28 Jul 2021 Article published 10.1186/s12920-021-01038-2

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