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Peer Review reports

From: Re-analysis of whole-exome sequencing data reveals a novel splicing variant in the SLC2A1 in a patient with GLUT1 Deficiency Syndrome 1 accompanied by hemangioma: a case report

Original Submission
27 Oct 2020 Submitted Original manuscript
15 Dec 2020 Reviewed Reviewer Report - Shameer Khadar
22 Feb 2021 Reviewed Reviewer Report
8 Mar 2021 Author responded Author comments - Tugce Bozkurt
Resubmission - Version 2
8 Mar 2021 Submitted Manuscript version 2
9 Mar 2021 Reviewed Reviewer Report - Shameer Khadar
23 Mar 2021 Reviewed Reviewer Report
2 Apr 2021 Author responded Author comments - Tugce Bozkurt
Resubmission - Version 3
2 Apr 2021 Submitted Manuscript version 3
9 Apr 2021 Author responded Author comments - Tugce Bozkurt
Resubmission - Version 4
9 Apr 2021 Submitted Manuscript version 4
16 Apr 2021 Author responded Author comments - Tugce Bozkurt
Resubmission - Version 5
16 Apr 2021 Submitted Manuscript version 5
Publishing
22 Jul 2021 Editorially accepted
31 Jul 2021 Article published 10.1186/s12920-021-01045-3

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